Oxidation Of Derivatives Research Articles

Synthesis and applications of metal oxide derivatives of ZIF-67: a mini-review

Metal–organic framework (MOFs) is a famous family of materials that have massive applications in material developments for diverse fields, including electronics, smart devices, catalysis, sensors, and separation technology. These materials get highlighted due to their defined morphology, structure, porous nature, and very extensive surface area available. There are various subclasses of MOFs, depending upon the metal cation and organic ligand present. ZIF-67 is one of the most extensively utilized MOF for various applications as a soft template. ZIF-67 displays characteristics of high catalytic activity, thermal and chemical stability, tuneable pore size, and so on, thus making it an attractive prospect for a number of research subjects as well as applications on a large scale. Moreover, combining the advantages of ZIF-67 with other components or structures result in compounds having potentially better performance than pure ZIF-67. Metal oxide nanoparticles/ZIF-67 is an emerging class of materials that holds functional distinctive properties. It unites the tailoring porosity of ZIF-67 with the diverse functionality of metal oxide crystalline structure. An extensive range of metal oxides/ZIF-67 have been integrated and their performance evaluated in applications like adsorption, catalysis, sensing, storage, microwave absorption, and so on. This review highlights the recent research fields where metal oxide nanoparticles derived from ZIF-67 have been critically applied, as also their synthesis strategies and morphological differences. ZIF-67 and its applications

Rapid Cycle Temperature Swing Adsorption Process Using Solid Structured Sorbent for CO2 capture from Cement Flue Gas

Concrete is the most widely used man-made material in the world. The production process of cement, a key component of concrete, contributes significantly to CO2 emissions. Every year, over 4 billion tonnes of cement are produced, releasing approximately 7%-8% of global CO2 emissions [1]. Cement flue gas, processes and raw materials, contain around 16% CO2 and 7-10% O2 and NOX /SOX (100-300 ppm), contingent on the fuel type. High amounts of NOX/SOX are a significant challenge for any carbon capture system. The presence of high O2 concentration in the emitted gas stream can chemically degrade typical amines via production of amides or other oxide derivatives. Therefore, it is crucial to conduct preliminary studies at a pilot scale using real cement flue gas conditions to develop a viable technology and accurate techno-economic analysis for large plants (1 million+ tonnes of captured CO2 per year). Svante (formerly Inventys) has a strong patent portfolio on Rapid Cycle Temperature Swing Adsorption (RC-TSA) processes using structured adsorbents, steam-assisted direct regeneration with fast kinetics (< 1.5 mins cycle time) as an alternative to traditional liquid amine technologies. This project utilized scaled up CALF-20 sorbent, one of the first Metal Organic Frameworks (MOFs) used in an industrial CO2 capture project. This MOF is robust with regards to steam, O2 and acidic contaminant gases (such a NOX/SOX) which make it an ideal candidate for the cement CO2 capture application. This article discusses efforts to scale up the CALF-20 MOF sorbent from lab scale to ton scale. A review of CALF-20 performance after 2300 hrs of VeloxoTherm™ capture process results on a boiler flue gas doped with CO2 and Air to simulate Cement kiln flue gas at 0.1 TPD capacity is presented. Also included are results from Phase 1 of the cement project related to NOX/SOX stability tests on CALF-20 sorbent.

BIOMARKERS OF OXIDATIVE STRESS IN THE MUSCLE TISSUE OF RAINBOW TROUT (ONCORHYNCHUS MYKISS WALBAUM) AFTER IN VITRO TREATMENT BY EXTRACTS DERIVED FROM STALKS AND ROOTS OF GREATER CELANDINE (CHELIDONIUM MAJUS L.)

Consistent with our previous studies, we continue to evaluate the antioxidant potential of Greater celandine (Chelidonium majus L), a representative of the Papaveraceae family, collected from northern Poland using the model of muscle tissue of rainbow trout (Oncorhynchus mykiss Walbaum). Therefore, in the present study, oxidative stress biomarkers [2-thiobarbituric acid reactive substances (TBARS), protein oxidative modification carbonyl derivative content, total antioxidant capacity (TAC)] were used to evaluate the antioxidant activity of extracts (final concentration 5 mg/mL) derived from stems and roots of C. majus. Rainbow trout muscle tissue was used in this study. Phosphate buffer was used as a positive control (blank). The results of the current study showed that stem and root extracts exhibited cytotoxic effects on cellular structures of muscle tissue by increasing the level of the lipid peroxidation biomarkers. These results suggest the possibility of using C. majus extract at 5 mg/mL as a source of pro-oxidant compounds and warrant further studies to evaluate their therapeutic potential. Levels of aldehydic and ketonic derivatives of oxidatively modified proteins and total antioxidant capacity were not significantly changed after in vitro incubation with the extracts derived from stalks and roots of C. majus. Screening of species of the family Papaveraceae for other biological activities, including antioxidant activity, is essential and may be effective in the search for preventive measures in the pathogenesis of some diseases, as well as in the prevention and treatment of some disorders in medicine and veterinary.

Photoinduced electron transfer in non-covalent complexes of C60 and phosphangulene oxide derivatives.

Investigation of photoinduced electron transfer (PET) in a series of experimentally reported complexes of fullerene with phosphangulene oxides shows that the replacement of O atoms in the bridge of phosphangulene with S atoms promotes efficient and ultrafast ET from phosphangulene oxide to fullerene in PGOOSS⊃C60 and PGOSSS⊃C60 complexes. The results obtained can be useful for the development of photovoltaic devices based on phosphangulenes.

Microwave-assisted Phospha-Michael addition reactions in the 13α-oestrone series and in vitro antiproliferative properties

Microwave-assisted phospha-Michael addition reactions were carried out in the 13α-oestrone series. The exocyclic 16-methylene-17-ketones as α,β-unsaturated ketones were reacted with secondary phosphine oxides as nucleophilic partners. The addition reactions furnished the two tertiary phosphine oxide diastereomers in high yields. The main product was the 16α-isomer. The antiproliferative activities of the newly synthesised organophosphorus compounds against a panel of nine human cancer cell lines were investigated by means of MTT assays. The most potent compound, the diphenylphosphine oxide derivative in the 3-O-methyl-13α-oestrone series (9), exerted selective cell growth-inhibitory activity against UPCI-SCC-131 and T47D cell lines with low micromolar IC50 values. Moreover, it displayed good tumour selectivity property determined against non-cancerous mouse fibroblast cells.

Acute and chronic effects of intravitreal bevacizumab on lung biomarkers of angiogenesis in the rat exposed to neonatal intermittent hypoxia

Purpose/Aim Intravitreal bevacizumab (Avastin) is an irreversible vascular endothelial growth factor (VEGF) inhibitor used to treat severe retinopathy of prematurity (ROP) in extremely low gestational age neonates (ELGANs). ELGANs who are at the highest risk for developing severe ROP often experience brief intermittent hypoxia (IH) episodes which may cause oxidative damage. We tested the hypothesis that intravitreal Avastin leaks into the systemic circulation during exposure to IH and has adverse effects on biomarkers of pulmonary microvascular maturation, thus leading to pulmonary hemorrhage and long-term pulmonary sequelae. Methods Neonatal rats at postnatal day (PN) 0 (birth) were exposed to either: 1) hyperoxia (50% O2) or 2) neonatal IH (50% O2 with brief episodes of 12% O2) from PN0 to PN14. Room air (RA) littermates served as controls. At PN14, the time of eye opening in rats, a single dose of Avastin (0.125 mg in 5 µL) was injected into the vitreous cavity of the left eyes. A control group received equivalent volume saline. At PN23 and PN45, blood gases, lung-to-body weight ratios, histology, immunofluorescence, and lung biomarkers of angiogenesis were examined. Results At PN23, Avastin increased lung VEGF, nitric oxide derivatives (NOx), and hypoxia-inducible factor (HIF)1a in the hyperoxia-exposed groups, but decreased soluble VEGFR-1 (sVEGFR-1). At PN45, lungs from animals exposed to neonatal IH and treated with Avastin were severely hemorrhagic with morphologic changes in lung architecture consistent with chronic lung disease. This was associated with higher VEGF and NOx levels, and lower insulin-like growth factor (IGF)-I and sVEGFR-1. Conclusions These findings prove our hypothesis that intravitreal Avastin penetrates the blood–ocular barrier in IH and alters lung biomarkers of angiogenesis. Avastin targeting of VEGF could affect normal lung development which may be exaggerated under pathologic conditions such as IH, ultimately leading to vascular permeability, vessel rupture, and pulmonary hemorrhage.

Graphene Oxides Derivatives Prepared by an Electrochemical Approach: Correlation between Structure and Properties.

Graphene oxide (GO) can be defined as a single monolayer of graphite with oxygen-containing functionalities such as epoxides, alcohols, and carboxylic acids. It is an interesting alternative to graphene for many applications due to its exceptional properties and feasibility of functionalization. In this study, electrochemically exfoliated graphene oxides (EGOs) with different amounts of surface groups, hence level of oxidation, were prepared by an electrochemical two-stage approach using graphite as raw material. A complete characterization of the EGOs was carried out in order to correlate their surface topography, interlayer spacing, defect content, and specific surface area (SSA) with their electrical, thermal, and mechanical properties. It has been found that the SSA has a direct relationship with the d-spacing. The EGOs electrical resistance decreases with increasing SSA while rises with increasing the D/G band intensity ratio in the Raman spectra, hence the defect content. Their thermal stability under both nitrogen and dry air atmospheres depends on both their oxidation level and defect content. Their macroscopic mechanical properties, namely the Young’s modulus and tensile strength, are influenced by the defect content, while no correlation was found with their SSA or interlayer spacing. Young moduli values as high as 54 GPa have been measured, which corroborates that the developed method preserves the integrity of the graphene flakes. Understanding the structure-property relationships in these materials is useful for the design of modified GOs with controllable morphologies and properties for a wide range of applications in electrical/electronic devices.

Efficacy and safety of inhaled nebulized sodium nitrite in asthmatic patients

BackgroundNitrite is a physiologic nitric oxide (NO) derivative that can be bioactivated to NO. NO has been shown to attenuate airway inflammation and enhance the anti-inflammatory effect of corticosteroids in the animal model of asthma. Here, we aimed to investigate the efficacy and safety of inhaled sodium nitrite as add-on therapy with inhaled corticosteroid (ICS) in adult patients with persistent asthma. MethodsIn protocol 1, 10 asthmatic patients were administered a single dose of nebulized 15-mg sodium nitrite to assess safety, effect on lung function, and pharmacokinetics of nitrite within 120 min. In protocol 2, 20 patients were randomly assigned to a nitrite (15 mg twice daily) group or a placebo group to assess the efficacy over 12 weeks. The primary outcome was the forced expiratory volume in 1 s (FEV1). The secondary outcomes were other lung function parameters, unplanned asthma-related visits at the emergency department (ED) or outpatient department (OPD), admission days, asthma control test (ACT), and safety. ResultsNebulized sodium nitrite had neither acute adverse effect nor effect on lung function test within 120 min. No blood pressure change was seen. At week 12, FEV1 increased in the nitrite group, whereas there was no change in the placebo group. There were 5 events of asthma exacerbation, 4 ED visits, and one unplanned OPD visit in the placebo group, but none of these was noted in the nitrite group. There was no change in ACT scores in both groups. No adverse event was reported during 12 weeks in the nitrite group. There was no change in methemoglobin levels and sputum inflammatory markers. ConclusionFrom our pilot trial, nebulized sodium nitrite is safe in asthmatic patients, and shows the potential to reduce asthma exacerbation compared with placebo.

Computational exploration of the 1,3‐dipolar cycloaddition reaction of 7‐isopropylidenebenzonorbornadiene with nitrile oxide and cyclic nitrone derivatives

AbstractThe synthesis of isoxazolidine and isoxazole derivatives, versatile building blocks for the construction of a wide range of complex heterocyclic architectures in synthetic organic and medicinal chemistry, is efficiently achieved via the 1,3‐dipolar cycloaddition reaction (1,3‐DC). Herein, we report an extensive theoretical study on the peri‐, regio‐, stereo, and enantio‐selectivities of 1,3‐DC of 7‐isopropylidenebenzonorbornadiene with nitrile oxide and cyclic nitrone derivatives using density functional theory calculations. Acetophenone‐substituted nitrile oxide periselectively adds across the endocyclic olefinic bond of the dipolarophile to furnish the exo‐cycloadduct as the major product, a reaction that has a rate constant of 1.88 × 109 s−1. The endo approach of this periselective path is the closest competing pathway with a rate constant of 4.59 × 107 s−1. Different substituents on the nitrile oxide do not affect the peri‐ and stereo‐selectivity of the reaction. Diethyl ether solvation has no substantial effect on the energetic patterns observed in the gas phase computation. Also, we report a novel 1,3‐DC between cyclic nitrone derivatives and 7‐isopropylidenebenzonorbornadiene as an efficient way to generate isoxazolidine derivatives. Even though the reactions of the cyclic nitrone derivatives have slightly higher activation barriers than the acyclic nitrile oxide derivatives, the former is more enantioselective than the latter. Whereas electron‐donating groups (EDGs) on the cyclic nitrone favor the formation of the exo‐cycloadduct, electron‐withdrawing groups (EWGs) favor the formation of the endo‐cycloadduct. Both 1,3‐dipoles add across the dipolarophile via a concerted asynchronous mechanism.

Immobilizing Polysulfide by In Situ Topochemical Oxidation Derivative TiC@Carbon-Included TiO2 Core-Shell Sulfur Hosts for Advanced Lithium-Sulfur Batteries.

The performance of lithium-sulfur (Li-S) batteries is greatly hindered by the notorious shuttle effect of lithium polysulfides (LiPSs). To address this issue, in situ topochemical oxidation derivative TiC@carbon-included TiO2 (TiC@C-TiO2 ) core-shell composite is designed and proposed as a multifunctional sulfur host, which integrates the merits of conductive TiC core to facilitate the redox reaction kinetics of sulfur species, and porous C-TiO2 shell to suppress the dissolution and shuttling of LiPSs through chemisorption. A unique dual chemical mediation mechanism is demonstrated for the proposed TiC@C-TiO2 composite that synergistically entraps LiPSs through thiosulfate/polythionate conversion coupled with strong polar-polar interaction. The morphological characterization reveals that the TiC@C-TiO2 -based cathode can well regulate the distribution of electrode materials to retard their accumulation inside the electrode, ensuring effective contact between the active materials and electrolyte. Based on its unique function and structure, the cathode delivers an improved capacity of 1256 mAh g-1 at 0.2C, a remarkable rate capability of 643 mAh g-1 , and an ultralow capacity decay rate of 0.065% per cycle at 2C over 900 cycles. This work not only demonstrates a dual chemical mediation mechanism to immobilize LiPSs, but also provides a universal strategy to construct multifunctional sulfur hosts for advanced Li-S batteries.

Estimation of Nitrite-Nitric Oxide Derivative-In Horses with Intestinal Colic by ESR Spectroscopy.

Diseases of the gastrointestinal tract of horses are caused by many factors and have a complex pathogenesis. Developing effective methods of differential diagnostics is of high fundamental and applied importance. The pathogenesis of diseases of the digestive tract of horses accompanied by the development of inflammation and oxidative stress, can be associated with a lack of the nitrogen monoxide which controls many signaling pathways in the body. The level of the nitric oxide (NO) is involved in the regulation of the immune and nervous systems, the tone of all the blood vessels, and the courses of many pathological processes. The nitric oxide activates guanylate cyclase (sGC) and leads to vascular relaxation. The aim of this investigation was to study the metabolites of nitric oxide in horses suffered from intestinal diseases. The levels of nitric oxide in the blood serum of horses depending on their age and health state was studied. The concentration of nitrites in the blood serum of horses aged 6–25 years was 3.4 ± 4.2 μM, and in the young horses (1–5 years) the level of this indicator was 8.2 ± 5.4 μM. A sharp decrease in nitrite was observed in all the horses with intestinal diseases of 2 ± 0.9 μM, especially with tympanitic caecun of 0.6 ± 0.4 μM and with spasmodic colic of 1.8 ± 0.5 μM. The level of nitrosylhemoglobin HbNO in the blood of the diseased animals was higher than that in clinically healthy horses, regardless of age.

A self-activating nanovesicle with oxygen-depleting capability for efficient hypoxia-responsive chemo-thermo cancer therapy

Hypoxia-activated prodrugs (HAPs) promise to mitigate side effects of conventional chemotherapy and to enable precise medication treatment. One challenge facing HAPs-based chemotherapy is prodrug failure in normoxic tumor region. However, current strategies to enhance tumor hypoxia rely on delivery of oxygen-consuming agents and external stimulation, which can impede the optimal application of HAPs. Herein, a novel self-activating nanovesicle, TH-302@BR-Chitosan NPs, is constructed by assembling bilirubin-chitosan conjugate (named as BR-Chitosan) with a HAP, TH-302. It is interesting to find that the BR-Chitosan shows the inherent oxygen-depleting performance, especially in the presence of over expressed H2O2 in tumor area, during which the BR-Chitosan can facily transform into biliverdin-chitosan (BV-Chitosan) and subsequently result in the disassembly of nanovesicles to release and activate the prodrug. Thus, this in situ strengthening hypoxia level of tumor can greatly promote the chemotherapy efficacy of HAPs. Moreover, as the oxidation derivatives of BR-Chitosan, BV-Chitosan exhibits intense absorbance at the range from long wavelength of visible region to near-infrared region, which can be acted as an effective photothermal agent for photothermal therapy (PTT). This biodegradable and self-activating nanovesicle with concise formulation demonstrates greatly enhanced synergistic therapeutic outcome in the activatable chemo-thermo combined therapy, showing much promising in future clinical transformation.

Cyclic DNA remethylation following active demethylation at euchromatic regions in mouse embryonic stem cells.

DNA methylation is an essential epigenetic mark that regulates normal mammalian embryonic development. DNA methylation profiles are not always static, especially during germline development. In zygotes, DNA is typically highly methylated but, during preimplantation, DNA methylation is erased globally. Then, at the start of post-implantation development in mouse embryos, DNA again becomes dramatically hypermethylated. Chromatin structure regulates the accessibility of DNA-modifying enzymes to target DNA. Beyond that, however, our understanding of the pathway by which chromatin regulation initiates changes in global DNA methylation during mouse embryonic development remains incomplete. To analyse the relationship between global regulation of DNA methylation and chromatin status, we examined 5-methylcytosine (5mC), modified by the DNA methyltransferase DNMT, and the oxidative derivative 5-hydroxymethylation (5hmC), converted from 5mC by TET-family enzymes, by means of immunofluorescence staining of mitotic chromosomes in mouse embryonic stem cells (ESCs). Our comparison of immunostaining patterns for those epigenetic modifications in wild-type, DNMT-deficient, and TET-deficient ESCs allowed us to visualise cell cycle-mediated DNA methylation changes, especially in euchromatic regions. Our findings suggest that DNA methylation patterns in undifferentiated mouse ESCs are stochastically balanced by the opposing effects of two activities: demethylation by TET and subsequent remethylation by DNMT.

5-Hydroxymethylation highlights the heterogeneity in keratinization and cell junctions in head and neck cancers

BackgroundHead and neck squamous cell carcinoma (HNSCC) is the sixth most prevalent cancer worldwide, with human papillomavirus (HPV)-related HNSCC rising to concerning levels. Extensive clinical, genetic and epigenetic differences exist between HPV-associated HNSCC and HPV-negative HNSCC, which is often linked to tobacco use. However, 5-hydroxymethylation (5hmC), an oxidative derivative of DNA methylation and its heterogeneity among HNSCC subtypes, has not been studied.ResultsWe characterized genome-wide 5hmC profiles in HNSCC by HPV status and subtype in 18 HPV(+) and 18 HPV(−) well-characterized tumors. Results showed significant genome-wide hyper-5hmC in HPV(−) tumors, with both promoter and enhancer 5hmC able to distinguish meaningful tumor subgroups. We identified specific genes whose differential expression by HPV status is driven by differential hydroxymethylation. CDKN2A (p16), used as a key biomarker for HPV status, exhibited the most extensive hyper-5hmC in HPV(+) tumors, while HPV(−) tumors showed hyper-5hmC in CDH13, TIMP2, MMP2 and other cancer-related genes. Among the previously reported two HPV(+) subtypes, IMU (stronger immune response) and KRT (more keratinization), the IMU subtype revealed hyper-5hmC and up-regulation of genes in cell migration, and hypo-5hmC with down-regulation in keratinization and cell junctions. We experimentally validated our key prediction of higher secreted and intracellular protein levels of the invasion gene MMP2 in HPV(−) oral cavity cell lines.ConclusionOur results implicate 5hmC in driving differences in keratinization, cell junctions and other cancer-related processes among tumor subtypes. We conclude that 5hmC levels are critical for defining tumor characteristics and potentially used to define clinically meaningful cancer patient subgroups.

Novel PDMS based semi-interpenetrating networks (IPNs) for the extraction of phenolic compounds

Four Semi-Interpenetrating Networks (semi-IPN) based on polydimethylsiloxane (PDMS) were developed for the sorptive extraction of polar phenolic compounds (log Kow ≤ 3). Their preparation is based on the hydrosilylation crosslinking reaction of dihydrosilane terminated polydimethylsiloxane with its homologue divinyl, followed by the addition of inert various polyethylene oxide derivatives (PEO). The physico-chemical properties of the semi-IPN were controlled by Differential Scanning Calorimetry (DSC), Scanning Electronic Microscopy (SEM), RAMAN spectroscopy and contact angle measurements, showing the homogeneity of the semi-IPN and their higher hydrophilicity. Under optimum extraction conditions of phenolic molecules as target analytes and using liquid chromatography as analysis techniques, the novel modified PDMS phases showed good extraction rate against polar analytes with an excellent relative recovery average (69–100 %) for phenolic molecules. The higher retention rates were obtained with 30 % interpenetrated copolymer PEO/PPO in PDMS. Moreover, five adsorption/desorption cycles led to a loss of 5.8 % of the adsorption efficiency, showing a good stability of these PDMS-based IPN phases.

Design and Synthesis of Solution-Processable Donor–Acceptor Dithienophosphole Oxide Derivatives for Multilevel Organic Resistive Memories

A class of solution-processable, donor–acceptor-decorated dithienophosphole oxide derivatives has been successfully synthesized and employed to fabricate solution-processed resistive memory devices...

Nanocomposite Coatings Based on Modified Graphene Oxide and Polydimethylsiloxane: Characterization and Thermal Properties

Graphene oxide as a derivative of graphite has been noticed as a high efficient material and its application in nanocomposite coatings is surprisingly increased. In this research, surface modification of graphene oxide using 3-aminopropyltriethoxysilane, as an aminic modifier, was done. Coating compositions based on polydimethylsiloxane containing graphene oxide and also modified graphene oxide were formulated and interaction of graphene oxide derivatives with siloxane polymer was evaluated using Fourier transform infrared spectroscopy – attenuated total reflectance, scanning electron microscopy, Atomic Force Microscopy, Raman spectroscopy and X-Ray Diffraction methods. Also thermogravimetric analysis and water contact angle tests were used for evaluation of thermal properties and hydrophobicity of resultant coatings, respectively. Results confirmed the interaction of graphene oxide with aminic modifier. Also, the presence of modified graphene oxide derivatives in the formulations led to the increase of thermal properties and hydrophobicity of the resultant coatings and the increase of these properties for formulations containing modified graphene was much greater and more pronounced.

The effects of the phthalate DiNP on reproduction†.

Di-isononyl phthalate (DiNP) is a high molecular weight, general purpose, plasticizer used primarily in the manufacture of polymers and consumer products. It can be metabolized rapidly and does not bioaccumulate. The primary metabolite of DiNP is monoisononyl-phthalate (MiNP) and the secondary metabolites include three oxidative derivatives of DiNP, which have been identified mainly in urine: mono-oxoisononyl phthalate (MOINP or oxo-MiNP), mono-carboxyisooctyl phthalate (MCIOP, MCOP or cx-MiNP), and mono-hydroxyisononyl phthalate (MHINP or OH-MiNP). The secondary metabolites are very sensitive biomarkers of DiNP exposure while primary metabolites are not. As the usage of DiNP worldwide increases, studies evaluating its potential reproductive toxicity are becoming more prevalent in the literature. In studies on female animals, the researchers found that the exposure to DiNP appears to induce negative effects on ovarian function and fertility in animal models. Whether or not DiNP has direct effects on the uterus is still controversial, and the effects on human reproduction require much more research. Studies on males indicate that DiNP exposure has disruptive effects on male reproduction and fertility. Occupational studies also indicate that the exposure to DiNP might induce negative effects on male reproduction, but larger cohort studies are needed to confirm this. This review presents an overview of the literature regarding the reproductive effects of exposure to DiNP.

Influence of Process Parameters on Countercurrent Reactor Reduction of Oxidized Mill Scale Waste and Its Co-relationship with Mathematical Model

Mill scale is treated as a waste product by the steel industry, so it is essential to recycle and reuse this waste for recovery of metallic iron and its single oxide derivative. Most of the study in the field of mill scale reduction focuses on the static mill scale reduction. Optimizing the process in dynamic conditions becomes more difficult because of the complexity involved inside the process. In the present method, mill scale having particle size ranges from 106 to 53 µm was converted to single-phase oxide Fe2O3 by blowing pure oxygen at 1100 °C and then it was subjected to a reducing atmosphere of 50% H2 and 50% N2 (1:1) at 875 ± 5 °C at a varying reactor angle from 2° to 5° and different mass flow rates varying from 0.037 to 0.148 kg/min. A generalized experimental model (GEM) has been formulated for the degree of reduction of oxide, which encompasses twelve parameters consisting of reactor design and process parameters. A Buckingham theorem was used to obtain dimensionless parameter for the degree of reduction, and a logical correlation using the proposed model has been established.

Directly application of bimetallic 2D-MOF for advanced electrocatalytic oxygen evolution

The development of non-noble oxygen evolution reaction (OER) catalysts with low energy consumption and cost is imperative to produce hydrogen energy from water splitting and enlarge its application. Two-dimensional (2D) metal organic frameworks (MOF) and their derivatives are widely regarded as promising electrocatalysts (EC) for OER due to its unique structural characteristics. Here, by optimizing the molar ratio of Ni to Co, bimetal 2-methylimidazole based 2D-MOF is synthesized and its derivatives are also obtained by phosphorization or oxidation. OER measurements prove that the original MOF structure with 5% Ni/Co molar ratio shows excellent activity with 310 mV overpotential (ƞ) at the current density of 10 mA cm−2 in 1 M KOH solution for OER, as well as a fairly good electrochemical stability rather than their oxidation or phosphorus derivatives. This work introduces a facile method to prepare bimetal imidazole-based 2D-MOF directly applied in energy conversion field without transformation, making a contribution for opening a new window of widely application of 2D-MOF and improving the hydrogen production efficiency from water splitting.