Formation Of Oxide Species Research Articles

FORMATION OF MULTINUCLEATED OSTEOCLASTS DEPENDS ON AN OXIDIZED SPECIES OF CELL SURFACE ASSOCIATED LA PROTEIN.

The bone-resorbing activity of osteoclasts plays a critical role in the life-long remodeling of our bones that is perturbed in many bone loss diseases. Multinucleated osteoclasts are formed by the fusion of precursor cells, and larger cells - generated by an increased number of cell fusion events - have higher resorptive activity. We find that osteoclast fusion and bone-resorption are promoted by reactive oxygen species (ROS) signaling and by an unconventional low molecular weight species of La protein, located at the osteoclast surface. Here, we develop the hypothesis that La's unique regulatory role in osteoclast multinucleation and function is controlled by a ROS switch in La trafficking. Using antibodies that recognize reduced or oxidized species of La, we find that differentiating osteoclasts enrich an oxidized species of La at the cell surface, which is distinct from the reduced La species conventionally localized within cell nuclei. ROS signaling triggers the shift from reduced to oxidized La species, its dephosphorylation and delivery to the surface of osteoclasts, where La promotes multinucleation and resorptive activity. Moreover, intracellular ROS signaling in differentiating osteoclasts oxidizes critical cysteine residues in the C-terminal half of La, producing this unconventional La species that promotes osteoclast fusion. Our findings suggest that redox signaling induces changes in the location and function of La and may represent a promising target for novel skeletal therapies.

Enhancing photocatalytic g-C3N4/PVDF membranes through new insights into the preparation methods

Fibrous membranes are crucial on the filtration of pollutants from air and water, but continued use can lead to a failure in effectiveness due to pollutant accumulation. To enhance durability, incorporating photocatalytic submicroparticles into these membranes appear as a solution.Here, we prepared a set of polyvinyl difluoride (PVDF) fibrous membranes modified with graphitic carbon nitride (g-C3N4) using three different methodologies. Their photocatalytic efficiency was investigated using phenol as model pollutant compound under visible light irradiation.Using g-C3N4 fibrous membranes modified by electrospinning blend a pseudo first-order kinetic constant (kapp) of 2.51 × 10-4 min-1 was observed for phenol degradation after 240 min reaction. Despite minimal particle adhesion the thermal treatment increased kapp to 5.41 × 10-4 min-1. The membranes prepared via chemical activation of PVDF exhibited the highest photocatalytic activity (kapp of 21.7 × 10-4 min-1). This superior activity was attributed to covalent bonds between PVDF and g-C3N4, allowing the formation of oxidative species.

Fabrication of new in‐situ ternary nano/microcomposite LDH/Ag2O/Bayerite in trimetallic NiAg/Al layered double hydroxides for CO2 capture material

AbstractWe reported new in‐situ ternary nano/microcomposite layered double hydroxides/Ag2O/bayerite in trimetallic NiAg/Al layered double hydroxides (LDH) via hydrothermal technique; and characterization by powder X‐ray diffraction (XRD), Fourier transforms infrared spectroscopy (FT‐IR), field emission scanning electron microscopy (FE‐SEM), energy dispersive spectroscopy (EDS), and N2 adsorption‐desorption. The formation of bayerite and silver oxide species on the LDH nanosheet depended on the excess of Al3+ and Ag+ in the solution under alkaline and hydrothermal conditions. The nitrogen isotherm adsorption profile for all ternary composites exhibited uniformity with mesoporous and lamellar characteristics. The surface area of all the composites ranged from 81.17 to 150.23 m2. g−1, the Barret‐Joyner‐Halenda (BJH) pore volume from 0.22 to 0.27 cm3. g−1, and the average pore diameter ranged from 3.47 to 5.78 nm. All composites show a laminar plate‐like structure covered with elongated pieces. The particle size of the composites ranged from 54.86 to 115.96 nm, indicating the size changed from nano to microcomposite because of the different molar ratios of Ag and Ni in the solid. The ternary composite reveals CO2 capture activity with adsorption capacity ranging from 13.93 to 19.61 mmol g−1. © 2024 Society of Chemical Industry and John Wiley & Sons, Ltd.

Metal–Organic Framework Fe-BTC as Heterogeneous Catalyst for Electro-Fenton Treatment of Tetracycline

This study explores the use of the iron-containing metal–organic framework (MOF), Basolite®F300, as a heterogeneous catalyst for electrochemically-driven Fenton processes. Electrochemical advanced oxidation processes (EAOPs) have shown promise on the abatement of recalcitrant organic pollutants such as pharmaceuticals. Tetracyclines (TC) are a frequently used class of antibiotics that are now polluting surface water and groundwater sources worldwide. Acknowledging the fast capability of EAOPs to treat persistent pharmaceutical pollutants, we propose an electrochemical Fenton treatment process that is catalyzed by the use of a commercially available MOF material to degrade TC. The efficiency of H2O2 generation in the IrO2/carbon felt setup is highlighted. However, electrochemical oxidation with H2O2 production (ECO-H2O2) alone is not enough to achieve complete TC removal, attributed to the formation of weak oxidant species. Incorporating Basolite®F300 in the heterogeneous electro-Fenton (HEF) process results in complete TC removal within 40 min, showcasing its efficacy. Additionally, this study explores the effect of varying MOF concentrations, indicating optimal removal rates at 100 mg L−1 due to a balance of kinetics and limitation of active sites of the catalysts. Furthermore, the impact of the applied current on TC removal is investigated, revealing a proportional relationship between current and removal rates. The analysis of energy efficiency emphasizes 50 mA as the optimal current, however, balancing removal efficiency with electrical energy consumption. This work highlights the potential of Basolite®F300 as an effective catalyst in the HEF process for pollutant abatement, providing valuable insights into optimizing electrified water treatment applications with MOF nanomaterials to treat organic pollutants.

The role of nitric oxide and hormone signaling in chronic stress, anxiety, depression and post-traumatic stress disorder

This paper provides a summary of the role of nitric oxide (NO) and hormones in the development of chronic stress, anxiety, depression, and post-traumatic stress disorder (PTSD). These mental health conditions are prevalent globally and involve complex molecular interactions. Although there is a significant amount of research and therapeutic options available, the underlying mechanisms of these disorders are still not fully understood. The primary pathophysiologic processes involved in chronic stress, anxiety, depression, and PTSD include dysregulation of the hypothalamic-pituitary-adrenal (HPA) axis, the intracellular influence of neuronal nitric oxide synthase (nNOS) on transcription factors, an inflammatory response with the formation of nitrergic oxidative species, and reduced serotonergic transmission in the dorsal raphe nucleus. Despite the extensive literature on this topic, there is a great need for further research to clarify the complexities inherent in these pathways, with the primary aim of improving psychiatric care.

Kinetic Insights into Boron-Based Materials Catalyzed Oxidative Dehydrogenation of Light Alkanes.

High selectivity toward alkenes in oxidative dehydrogenation (ODH) of light alkanes makes boron-based materials promising catalysts. However, many key mechanistic aspects are still debated due to the challenge of capturing fleeting reaction intermediates. Kinetic analysis, including determining reaction orders and activation energy, could be informative for reactions involving radical intermediates but has not been extensively exploited. This Review summarizes the current understanding of the apparent alkane reaction order and the apparent activation energy in the boron-catalyzed ODH. Despite varying compositions and structures, a majority of boron-based catalysts share many common features, including alkene selectivity, the evolution and the formation of active site, and the apparent kinetic properties. These common trends could be attributed to the shared gas-phase radical-mediated reaction pathways and the formation of active hydroxylated boron oxide species on boron-containing materials under ODH conditions. Values of apparent alkane reaction orders and apparent activation energies are sensitive and reliable experimental measures of the contributions of the gas-phase radical-mediated and surface-mediated pathways, suggesting the outline of a general mechanistic framework of the boron-catalyzed ODH.

In-situ preparation of Ni@ZrO2 nanocapsules powder by DC arc plasma for internal electrode of MLCC

Zirconium oxide-coated Ni nanocapsules (Ni@ZrO2 NCs) were in-situ fabricated by DC arc plasma in a nitrogen atmosphere. The co-evaporation of a target mixture consisting of coarse ZrO2 and Ni powders resulted in the formation of Ni@ZrO2 core-shell nanocomposites (NCs). The high energy states of excited ions (Ni3+, Zr4+, O2−, N2+, etc.) within the arc plasma region were recorded in real time by online optical emission spectroscopy (OES), which becomes visible evidences of the energy conditions for the fabrication of Ni@ZrO2 NCs. These nanocapsules underwent preferential formation of zirconium oxide species based on the oxygen potential rule, followed by the nucleation and subsequent growth processes. The Ni@ZrO2 NCs exhibited improved oxidation resistance, with an onset temperature for sintering approximately 40 °C higher than that of pristine Ni nanoparticles (NPs). Additionally, these NCs displayed an appropriate shrinkage rate, with a volume change of about 7.1% at 1200 °C. The symbiotic relationship between the ZrO2 shell and the Ni core within each nanoparticle suggests enhanced interfacial stability, rendering these NCs a promising material for the advancement of multi-layer ceramic capacitors (MLCCs).

Radical-driven selective oxidation of benzyl alcohol on MnCoOx catalysts with no oxidant other than air in reactor

Mn reinforced Co3O4 catalysts (MnCoOx) were prepared by a facile solid phase mixed foaming method with an in-situ heating enhancement for the formation of spinel phase mixed oxide species, and studied in the selective oxidation of benzyl alcohol just the air in reactor as oxygen donor. It was found that the MnCoOx catalysts are composed of relatively minimal spinel MnCo2O4 mixed oxide and massive Co3O4 to form MnCo2O4-Co3O4 oxide pair. The micro-domains of MnCo2O4-Co3O4 oxide pair present two redox couples of Mn3+/Mn2+ and Co3+/Co2+ instead of the single one of Co3+/Co2+ in Co3O4, and then dramatically enhance the formation of superoxide radicals (•O2–) species from the O2 in air, which can efficiently initiate the conversion of benzyl alcohol to benzaldehyde in a Fenton-like processes. With no oxidant other than air in reactor, the interaction between MnCo2O4 and Co3O4 in MnCoOx catalysts leads to a benzyl alcohol conversion up to 98 % with a 100 % benzaldehyde selectivity at atmospheric pressure while single component Co3O4 can only present a benzyl alcohol conversion at 37 %. This embodiment of highly efficient heterogeneous selective oxidation just with air as oxidant provides a probability for developing a low-cost and super-facile radical-induced selective oxidation process for alcohols.

Effect of Ag and Ni-Doped Cerium Oxide Nanoparticles on the Formation of ROS and Evaluation as an Alternative Physical Sunscreen Material.

CeO2 nanoparticles (nanoceria) were proposed as an alternative physical sunscreen agent with antioxidant properties and comparable UV absorption performance. Green synthesis of nanoceria with Ag and Ni dopants resulted in doped nanoceria with lower catalytic activity and biologically-safe characteristics. The doped nanoceria was characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM), Rancimat Instrument, and UV-Vis Spectrophotometer for SPF (Sun Protection Factor) determination. XRD and TEM analysis showed that nanoceria had been successfully formed in nanoscale-sized with a change in crystallite size due to the crystal defect phenomenon caused by dopant addition. While the Rancimat test and band gap energy analysis were conducted to evaluate the oxidative stability and reactive oxygen species formation, it was confirmed that dopant addition could decrease catalytic activity of material, resulting in Ni-doped Ce with a longer incubation time (11.81 h) than Ag-doped Ce (10.58 h) and non-doped Ce (10.30 h). In-vitro SPF value was measured using the thin layer technique of sunscreen prototype with Virgin Coconut Oil (VCO)-based emulsion, which yielded 10.862 and 5.728 SPF values for 10% Ag-doped Ce and 10% Ni-doped Ce, respectively. The dopant addition of nanoceria could reduce catalytic activity and give a decent in vitro UV-shielding performance test; thus, Ag and Ni-doped nanoceria could be seen as promising candidates for alternative physical sunscreen agents.

Influence of the argon admixture on the reactive oxide species formation inside an atmospheric pressure oxygen plasma jet

In this work, a new atmospheric pressure plasma generated in a wire-to-multiwire dielectric barrier discharge on pure oxygen is introduced. This special geometry of 13 wires (one central wire and 12 ones on the external tube) is feeding by a radio frequency (RF) power (13.56 MHz, 1 kW) and produces a stable discharge. The capacity of this device to produce oxygen reactive species and the influence of Ar gas mixture (1–3%) on this production are investigated. The main characteristics of this DBD plasma are measured using optical emission spectroscopy techniques. The rotational, vibrational, and excitation temperatures along with the electron density are determined from OH (A2Σ → X2Π) band and the Stark broadening of the hydrogen atomic line at 486.1 nm, respectively. The temporal evolution and spatial distribution of charged and reactive species in this plasma are also numerically studied by a Global scheme and a two-dimension fluid model based on drift–diffusion approximation. A kinetic dominated by electron collisions is obtained for this plasma. The generation and movement of electrons, positive and negative ions in the wire-to-multiwire configuration are analyzed and discussed according to changes the electric field and plasma frequency. It is shown that the density of both charged and reactive species increases by adding a small amount of argon to the oxygen plasma while the electron temperature reduces in this configuration. A high level of agreement is observed between the experimental and simulation results for the electron density and temperature in this DBD plasma.

Dry reforming of methane over gallium-based supported catalytically active liquid metal solutions

Gallium-rich supported catalytically active liquid metal solutions (SCALMS) were recently introduced as a new way towards heterogeneous single atom catalysis. SCALMS were demonstrated to exhibit a certain resistance against coking during the dehydrogenation of alkanes using Ga-rich alloys of noble metals. Here, the conceptual catalytic application of SCALMS in dry reforming of methane (DRM) is tested with non-noble metal (Co, Cu, Fe, Ni) atoms in the gallium-rich liquid alloy. This study introduces SCALMS to high-temperature applications and an oxidative reaction environment. Most catalysts were shown to undergo severe oxidation during DRM, while Ga-Ni SCALMS retained a certain level of activity. This observation is explained by a kinetically controlled redox process, namely oxidation to gallium oxide species and re-reduction via H2 activation over Ni. Consequentially, this redox process can be shifted to the metallic side when using increasing concentrations of Ni in Ga, which strongly suppresses coke formation. Density-functional theory (DFT) based ab initio molecular dynamics (AIMD) simulations were performed to confirm the increased availability of Ni at the liquid alloy-gas interface. However, leaching of gallium via the formation of volatile oxidic species during the hypothesised redox cycles was identified indicating a critical instability of Ga-Ni SCALMS for prolonged test durations.

Selective cracking of light cycle oil to monoaromatics over non-noble bifunctional zeolite-supported Ni and NiW catalysts

The utilization of light cycle oil (LCO) for producing monoaromatics is investigated using bifunctional Ni and NiW catalysts supported on four different zeolites at atmospheric pressure without using external H2. The order of BTX yield for various feed compositions (2-methylnaphthalene, 2-methylnaphthalene + 9-methylanthracene, LCO) is: NiW/Beta > NiW/Y > Ni/Beta > NiW/Mordenite > Ni/Y > NiW/Mix > Ni/Mordenite > Ni/Mix, whereas the coke yield exhibits the reverse trend. The better performance of NiW-based catalysts is explained by the formation of NiW oxide species and their strong interactions with the support, as ascertained through H2-TPR, XPS, and UV-DRS. The higher moderate acidity, optimal balance between medium-strength Brønsted acid sites (BAS) and strong Lewis acid sites (LAS), and the higher hydrogen transfer index (HTI) in NiW-based catalysts, facilitate the selective cracking of LCO, resulting in the desired product yield. This study also establishes a strong correlation between the structural properties of various catalysts (pore diameter, surface area, pore volume, crystallite size) and the performance parameters, thus explaining the superior performance of Beta zeolite-supported catalysts for BTX production. Experiments with NiW/Beta and a physical mixture of W/Beta and Ni/Beta show the synergistic effect due to the co-presence of Ni and W. It is inferred that triaromatics are rapidly transformed to diaromatics, and the conversion of monoaromatics having two rings determines the BTX yield. LCO compounds are found to be the primary source for the formation of monoaromatics, while n-hexadecane (n-HD) is the hydrogen source. Reaction pathways for 2-methylnaphthalene and 9-methylanthracene conversion are presented based on detailed product characterization.

Iron-promoted zirconia-alumina supported Ni catalyst for highly efficient and cost-effective hydrogen production via dry reforming of methane

Developing cost-effective and high-performance catalyst systems for dry reforming of methane (DRM) is crucial for producing hydrogen (H2) sustainably. Herein, we investigate using iron (Fe) as a promoter and major alumina support in Ni-based catalysts to improve their DRM performance. The addition of iron as a promotor was found to add reducible iron species along with reducible NiO species, enhance the basicity and induce the deposition of oxidizable carbon. By incorporating 1 wt.% Fe into a 5Ni/10ZrAl catalyst, a higher CO2 interaction and formation of reducible "NiO-species having strong interaction with support" was observed, which led to an ∼80% H2 yield in 420 min of Time on Stream (TOS). Further increasing the Fe content to 2wt% led to the formation of additional reducible iron oxide species and a noticeable rise in H2 yield up to 84%. Despite the severe weight loss on Fe-promoted catalysts, high H2 yield was maintained due to the proper balance between the rate of CH4 decomposition and the rate of carbon deposit diffusion. Finally, incorporating 3 wt.% Fe into the 5Ni/10ZrAl catalyst resulted in the highest CO2 interaction, wide presence of reducible NiO-species, minimum graphitic deposit and an 87% H2 yield. Our findings suggest that iron-promoted zirconia-alumina-supported Ni catalysts can be a cheap and excellent catalytic system for H2 production via DRM.

Effect of sodium hypochlorite as a depressant for copper species in Cu-Mo flotation separation

One alternative to replace conventional depressants in Cu-Mo separation is using oxidizing agents to promote the formation of products on chalcopyrite that render its surface hydrophilic and thus favor its depression. This work provides a study to understand how sodium hypochlorite can act as a depressor for chalcopyrite in Cu-Mo flotation separation. The effect of NaClO in flotation tests was evaluated by means of electrochemical techniques, scanning electron microscopy (SEM), Fourier transform infrared analysis and contact angle measurements. The flotation results showed a selective depressant effect at a dosage of 1,020 g/t NaClO, conditioning time of 5 min, and pH 7. The mixed potential showed that the oxidation of chalcopyrite and molybdenite is possible through the addition of NaClO. The SEM observations showed changes in oxidized chalcopyrite morphology, which is supported by the decreasing contact angle change; no morphological changes were observed on molybdenite. FTIR analyses showed the characteristic peaks of the OH group after chalcopyrite was treated with NaClO; when molybdenite was treated with NaClO, the FTIR spectrum did not show changes. A scheme is proposed for the formation of oxidation species.

Catalytic Oxidation of VOC over Cobalt-Loaded Hierarchical MFI Zeolite

The zeolites ZSM-5 with different Si/Al ratios were modified with a buffer solution of HF and NH4F. This acidic treatment led to the obtaining of a material with secondary mesoporosity. The deposition of cobalt from an aqueous solution of cobalt acetate on the surface of treated samples generates the formation of different cobalt oxide species: bulk-like Co3O4 phases strongly interacting with the support, Co2+ in ion exchange positions (γ and β sites) and silicate-like phases. The mechanism of cobalt silicate phase formation is proposed here and includes a replacement of silanol groups and the bridging hydrogens by Co and the inclusion of the Co atoms in tetrahedral framework positions. The catalysts, obtained through use of the treated ZSM-5, exhibit higher activity in the reactions of propane, and n-hexane completes oxidation compared with the catalyst samples containing un-treated zeolite. Both the finer dispersion of metal oxide particles on the hierarchical sample and the presence of secondary mesoporosity improve the effectiveness of the active phase utilization via access to larger number of active sites.

Activation of periodate with pinewood biochar-CuO composite for the removal of recalcitrant organic pollutants – Mechanisms and degradation products

The degradation kinetics and mechanisms of various types of recalcitrant organic pollutants (ROPs) by a novel biochar-CuO (B-CuO)/periodate (PI) system have been deeply investigated in the present study. More precisely, the study aimed to explore the significant effects of pH on the formation of various oxidative species using this treatment system. According to the results achieved, iodate (IO3∙) and periodate radicals (IO4∙), ∙OH and O(3P) were mostly generated at pH ≈ 7, resulting in the efficient removal of methylene blue (MB) (90% after 30 min, kobs = 0.09 min−1), while the system favoured the formation of O(3P) under highly alkaline pH values (pH = 11), leading to lower degradation kinetics of the pollutant (51% after 30 min, kobs = 0.028 min−1). Additionally, no oxidative species were found at highly acidic pH values (pH = 3), and no significant MB removal was observed (21% after 30 min, kobs = 0.0081 min−1). Elevating the temperature (from 25 °C to 80 °C) and bubbling with nitrogen or oxygen gas also did not have any significant effects on the degradation of ROPs. Additionally, the system maintained its efficiency in various water matrices, including real wastewater, confirming the applicability of the biochar-CuO/PI system for real water treatment processes. The system also exhibited a high degradation efficiency for other types of ROPs, such as ciprofloxacin. Experiments using ultra-high performance liquid chromatography in combination with quadrupole time-of-flight mass spectrometry were performed to identify the degradation products and pathways of MB, revealing the contribution of two different degradation pathways and the formation of five degradation products in the B-CuO/PI system. The ECOSAR program was employed to evaluate the predicted toxicity of the degradation products. The results showed that the system could efficiently detoxify MB.

Simultaneous hydrodynamic cavitation and glow plasma discharge for the degradation of metronidazole in drinking water

In this study, a novel hydrodynamic cavitation unit combined with a glow plasma discharge system (HC-GPD) was proposed for the degradation of pharmaceutical compounds in drinking water. Metronidazole (MNZ), a commonly used broad-spectrum antibiotic, was selected to demonstrate the potential of the proposed system. Cavitation bubbles generated by hydrodynamic cavitation (HC) can provide a pathway for charge conduction during glow plasma discharge (GPD). The synergistic effect between HC and GPD promotes the production of hydroxyl radicals, emission of UV light, and shock waves for MNZ degradation. Sonochemical dosimetry provided information on the enhanced formation of hydroxyl radicals during glow plasma discharge compared to hydrodynamic cavitation alone. Experimental results showed a MNZ degradation of 14% in 15 min for the HC alone (solution initially containing 300 × 10−6 mol L−1 MNZ). In experiments with the HC-GPD system, MNZ degradation of 90% in 15 min was detected. No significant differences were observed in MNZ degradation in acidic and alkaline solutions. MNZ degradation was also studied in the presence of inorganic anions. Experimental results showed that the system is suitable for the treatment of solutions with conductivity up to 1500 × 10−6 S cm−1. The results of sonochemical dosimetry showed the formation of oxidant species of 0.15 × 10−3 mol H2O2 L−1 in the HC system after 15 min. For the HC-GPD system, the concentration of oxidant species after 15 min reached 13 × 10−3 molH2O2L−1. Based on these results, the potential of combining HC and GPD systems for water treatment was demonstrated. The present work provided useful information on the synergistic effect between hydrodynamic cavitation and glow plasma discharge and their application for the degradation of antibiotics in drinking water.

Highly Efficient Copper Doping LaFeO3 Perovskite for Bisphenol A Removal by Activating Peroxymonosulfate

A series of copper doping LaFeO3 perovskite (LaCuxFe1−xO3, LCFO, x = 0.1, 0.4, 0.5, 0.6, 0.9) are successfully synthesized by the sol-gel method under mild conditions. In this study, it is applied for the activation of peroxymonosulfate (PMS) for bisphenol A (BPA) removal. More than 92.6% of BPA was degraded within 30 min at 0.7 g/L of LCFO and 10.0 mM of PMS over a wide pH range with limited leaching of copper and iron ions. The physical–chemical properties of the catalysts were demonstrated by using X-ray diffraction (XRD), N2 adsorption–desorption isotherms, scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). Furthermore, the effects of catalyst dosage, PMS concentration, initial pH value, and inorganic anions on the LCFO/PMS system were fully investigated. Quenching experiments were performed to verify the formation of reactive oxidant species, which showed that the radical reaction and mechanisms play a great role in the catalytic degradation of BPA. The perovskite LCFO is considered a stable, easy to synthesize, and efficient catalyst for the activation of PMS for wastewater treatment.

Physiological Toxicity and Antioxidant Mechanism of Photoaging Microplastics on Pisum sativum L. Seedlings.

Recent studies have confirmed that changes in the physical properties of microplastics (MPs) trigger toxicological effects and ecological risks. To explore the toxicity of different types of MPs on plants, and the influence of MP photoaging, this study investigated the toxicity mechanisms of pristine, 7 and 14 d photoaged polystyrene (PS), polyamide (PA), polyethylene (PE), and polyethylene terephthalate (PET) MPs on seed germination, root growth, nutrient fraction, oxidative stress, and antioxidant systems of Pisum sativum L. (pea) seedlings. The results showed that pristine PS and 14 d photoaged PET inhibited seed germination. Compared to the pristine MPs, photoaged MPs had negative effects on root elongation. Moreover, photoaged PA and PE impeded the nutrient transport of soluble sugars from roots to stems. Notably, the production of superoxide anion radicals (•O2-) and hydroxyl radicals (•OH) through the photoaging of MPs exacerbated oxidative stress and reactive oxygen species formation in roots. Antioxidant enzyme data revealed that the activities of superoxide dismutase and catalase were significantly activated in photoaged PS and PE, respectively, in order to scavenge •O2- and hydrogen peroxide (H2O2) accumulation and alleviate lipid peroxidation levels in cells. These findings provide a new research perspective on the phytotoxicity and ecological risk of photoaged MPs.

Effect of organic phosphorus addition on the state of active metal species and catalytic performance of NiW/Al2O3 hydrodesulfurization catalyst

This article proposes a novel organic additive 1-hydroxyethylidene-1,1-diphosphonic acid (HEDP) for the preparation of NiW/Al2O3 efficient hydrodesulfurization (HDS) catalysts. The effects of HEDP on the nature of the tungsten and nickel species supported on the support surface after drying and calcination steps were revealed by employing ultraviolet–visible spectroscopy (UV–Vis), Raman spectroscopy, N2 adsorption–desorption and H2 temperature programmed reduction (H2-TPR). While the slab morphology and the proportion of NiWS phases were determined by X-ray photoelectron spectroscopy (XPS) and high-resolution transmission electron microscopy (HRTEM). Finally, dibenzothiophene (DBT) was used as a probe to evaluate the effects of HEDP modification on the catalytic performance of the prepared catalyst. The results indicate that the addition of HEDP can facilitate the formation of more polymerized tungsten oxide species and improve the availability of surface nickel atoms. The weakened interaction between active metals and support generate higher stacking numbers and shorter slab lengths among WS2 crystals on the corresponding catalyst, promote the sulfidation of both Ni and W species and enhance the proportion of NiWS phase. The catalytic evaluation results show that the HEDP-modified catalyst exhibits efficient HDS activity and higher DDS selectivity compared to the phosphoric acid-modified reference catalyst, which is attributed to a large number of accessible NiWS active sites. The present work relates the addition of organic additives with the formation of NiW species and the catalytic activity. The results highlight that the addition of HEDP is an effective strategy to improve the performance of HDS catalysts.