Reduction Process Research Articles

Hydrogen reduction and baking process of Pb-silicate microchannel plate and their performance studies

Microchannel plate (MCP) are honeycomb structures consisting of numerous parallel, hollow micro glass fiber channels renowned for their exceptional secondary electron multiplication. This paper investigates changes in MCP properties under hydrogen reduction temperatures ranging from 300 °C to 500 °C. The findings reveal that higher temperatures reduce surface metal oxides, which then accumulate within and darken the microchannels, affecting electron transport. Bulk resistance decreases before increasing, while gain increases and then decreases. At 350 °C, lead oxide begins to reduce to its conductive state, enhancing electron multiplication. However, increased temperatures cause clustering and roughening of the inner channel walls, which diminishes the efficiency of secondary electron release. These alterations are associated with the reduction dynamics of lead ions and temperature-induced microstructural changes. As the hydrogen reduction temperature increases, internal stresses shift outward, and the uniformity of gain varies, reaching its peak at 400 °C. Additionally, an aluminum oxide film enhances resistance to baking and ensures consistent bulk resistance. This study elucidates the relationship between MCP performance and reduction temperature, providing valuable insights for design improvement.

Efficient removal of Cr(VI) containing tunnel wastewater by sludge biochar loaded with ferrous sulfate

The ease of agglomeration reduced the removal of pollutants by FeS particles. Hence, sludge biochar was employed as a support to produce FeS-loaded biochar composites (FeS@BC) using a solvothermal method, for removing Cr(VI) from wastewater. The performance and mechanism of Cr(VI) removal on FeS@BC were investigated through adsorption experiments and characterization techniques. The adsorption tests revealed that under optimal conditions of solution pH of 3 and dosage of 40 mg, FeS@BC achieved a removal efficiency of over 97 % for 50 mg/L Cr(VI). The presence of Cl- and NO-3 did not affect Cr(VI) removal, whereas sulfate, phosphate, and carbonate inhibited the removal process. Low concentrations of humic acid (1–5 mg/L) held a negligible influence on removing, but elevated concentrations of humic acid inhibited Cr(VI) removal. The behavior of FeS@BC in removing Cr(VI) complied with to the pseudo-second-order and the Langmuir model. At 308.15 K, the largest removal capability of FeS@BC for Cr(VI) reached 185.874 mg/g. Thermodynamic studies confirmed that the Cr(VI) removing processes on FeS@BC were a spontaneous, entropy-driven, endothermic chemical adsorption. The primary mechanism for removing Cr(VI) on FeS@BC included reduction, electrostatic adsorption, complexation, and precipitation, with the reduction process playing a crucial role. This indicated that sludge biochar loaded with FeS was an ideal material for removing Cr(VI) from wastewater.

Green synthesis of copper nanoparticles from Terminalia arjuna (L.) bark extract: Characterization and potential for mercury degradation

The focus of this study is on synthesizing copper nanoparticles through a green approach, utilizing Terminalia arjuna bark extract. The ultra violet (UV) spectral analysis of copper nanoparticles synthesized through environmentally friendly methods revealed distinct absorption peaks at 287 nm, 575 nm, and 898 nm, indicative of significant light absorption. These peaks elucidate the nanoparticles' optical characteristics, shedding light on electronic transitions and surface plasmon resonance phenomena. Fourier transform infrared spectroscopy (FTIR) analysis displayed various peaks, suggesting vibrations associated with copper nanoparticles and functional groups in T. arjuna bark extract. The X-ray diffraction analysis (XRD) data exhibited characteristic peaks corresponding to metallic copper's crystallographic planes, confirming the formation of highly crystalline copper nanoparticles. Atomic force microscopy results depicted surface morphology and particle size distribution. Copper nanoparticles show promise in mercury degradation due to their high surface area and catalytic activity. They interact effectively with mercury ions through adsorption, reduction, and oxidation processes, leading to sequestration or transformation into less toxic forms. Functionalization enhances their affinity towards mercury, while synergies with other nanomaterials boost efficiency. Green synthesized copper nanoparticles offer an eco-friendly solution for effective mercury remediation, promising advancements in sustainable nanotechnological approaches for global environmental sustainability. KEY WORDS: Mercury, Copper, Terminalia arjuna, Remediation Bull. Chem. Soc. Ethiop. 2024, 38(6), 1703-1713. DOI: https://dx.doi.org/10.4314/bcse.v38i6.16

Conductive Li2S‐NbSe2 Cathode Material Capable of Bidirectional Self‐Activation for High‐Performance All‐Solid‐State Lithium Metal Batteries

AbstractAll‐solid‐state lithium metal batteries (ASSLBs) offer an alternative route to safe and high energy density power sources. Sulfur‐based cathodes with high theoretical specific capacity and low cost are crucial for advancing ASSLBs. However, the electronic insulation and sluggish kinetics of sulfide materials like Li2S severely limit battery performance. Herein, the strategy is proposed that a highly electronic conductive Li2S‐NbSe2 material enhances the electrochemical performance through bidirectional self‐activation. The chemical interaction between Li2S and NbSe2 induces NbSe2‐xSx and Li2Se derivatization, serving as the basis for activation. The carrier transport properties, chemical evolution and self‐activation mechanism of Li2S‐NbSe2 during the oxidation–reduction process are revealed. The chemical activation of NbSe2‐xSx is explored to accelerate the electrochemical processes by modifying the conductivity of sulfur species and the conversion pathways without insulating Li2S and S aggregation. Therefore, ASSLBs using Li2S‐NbSe2 as cathode active material achieve an electrode‐level energy density of 394 Wh kg−1 and a power density of 524 W kg−1 at 1 C (4.35 mA cm−2) and 25 °C. The capacity retention after 100 cycles at 0.5 C is ≈99.3% with almost no degradation. This work provides new options and insights for the rational design and development of chalcogenide cathode active materials for high‐performance ASSLBs.

Activating colloidal synthesized Au catalyst by the electrochemical strategy: Gas atmosphere, electrolyte and electrochemical technique

Organic ligands are necessarily used to stabilize nanoparticles (NPs) in colloid synthesis, and the presence of these ligands in most cases can have adverse effects on heterogeneous nanocatalysis. Therefore, it is crucial to develop efficient methods to remove ligands and study the removal mechanism. In this article, we developed a combined electrochemical method (chronoamperometry (CA) + cyclic voltammetry (CV)), which can completely and efficiently remove thiol ligand from Au NPs to produce cleaned Au/C catalyst. Using the oxygen reduction reaction (ORR) activity as the evaluation criterion for ligand removal, we found that gas atmosphere (O2) plays an important role in the removal process, while the acidity and alkalinity of electrolyte have no effect on the removal efficiency. A proposed thiol ligand removal mechanism along with Au degradation is presented. The results of CA activation at an oxidation constant potential (1.7 V) indicate that oxidation of thiol alone cannot remove thiol ligand. Only if a reduction constant potential of 0.2 V is further applied, the ORR activity of Au/C catalyst will increase, indicating that both the oxidation and reduction processes of Au NPs are crucial for ligand removal. Although the CA method (with an upper potential of 1.7 V and a lower potential of 0.2 V) can efficiently remove the majority of thiol ligand, complete removal of thiol ligand requires further CV activation. Based on the relevant results, a combined electrochemical method (CA + CV) is established. Developing standardized methods for removing ligands on the surface of catalysts is important for obtaining efficient catalysts and is also important for the reproducibility of catalytic results.

Флюидный режим образования вторичных доломитов в палеозойских карбонатных коллекторах Хасырейского месторождения (вал Гамбурцева)

The search for hydrocarbon deposits in the sediments of the Lower Paleozoic complex of the Timan-Pechora oil and gas province, which are associated with the main prospects for increasing reserves, is a relevant topic for research. It is necessary to understand the formation processes of carbonate reservoirs within the complex under consideration to develop a strategy for predicting the structure of the complex reservoirs. Obtaining data on the parameters of the fluid regime of the formation of secondary dolomites in the Paleozoic carbonate reservoirs of the Khasyrey field (Gamburtsev swell) was the aim of the study. We studied primary fluid inclusions in dolomite and anhydrite cements filling vuggy voids in reservoir rocks. We showed that the inclusions contained up to 10 vol. % of the gas phase, which was represented by methane and water vapor. The liquid phase was characterized by a substantially chloride-calcium composition, the salinity is 13.5–23.5 wt. % NaCl-eq. These data might indicate the formation of cavities and cements of secondary dolomites from moderate-temperature solutions of high salinity, which were formed as a result of mixing sedimentation (primary marine) waters and brines of hydrothermal vents. The products of evaporite dissolution in the presence of hydrocarbons and sulfate reduction processes were the most likely source and supplier of the fluids, both the formation of leaching caverns in the rock and the cements performing them. Fluids could enter the upper floors of the section from hydrothermal sources in the basement zones and lower horizons of the sedimentary cover through a system of faults and cracks during tectonic activation.

Low-energy argon ion beam irradiation for the surface modification and reduction of graphene oxide: Insights from XPS

Developing environmentally friendly methods for reducing graphene oxide (GO) is essential. This study investigates the surface modification and reduction of GO films using 200 eV argon ion (Ar+) beam irradiation. X-ray Photoelectron Spectroscopy (XPS) analysis reveals significant chemical changes on the GO surface. GO was irradiated with a 200 eV Ar+beam for varying times (0–80 s). XPS survey spectra showed the presence of carbon and oxygen, with an increasing carbon atomic percentage over time. High-resolution XPS spectra of C 1s revealed peaks corresponding to sp2, C–OH, O–C–O, CO, and O–CO bonds. In the O 1s spectra, CO, O–C–O, and C–OH groups were observed. Upon irradiation, the CO peak consistently decreased, the O–C–O peak fluctuated, and the C–OH peak increased, indicating effective reduction of CO groups, dynamic changes in O–C–O functionalities, and the formation of additional C–OH groups. The C/O ratio increased from ∼2.4 to 2.7, underscoring the reduction process and enhanced carbon content. This method proves to be an efficient approach for producing reduced graphene oxide (rGO) with improved properties for advanced applications.

Manufacturing of heavy tungsten alloys from nano-sized metal oxides via simultaneous reduction-sintering powder treatments

Heavy tungsten alloys are of great importance in the engineering and mining industries as well as the military and medical applications because of their stability at high temperatures, high strength and dense structures. The present study develops a novel technology for the production of heavy tungsten alloys via thermal treatment of nano-sized metal oxides based on simultaneous reduction and sintering processes. Heavy tungsten alloy (95W-3Ni-2Fe) was produced from the reduction of mixed nano-sized metal oxides precursor in H2 at 1000 o C followed by sintering at 1350–1450 o C for 30–90 min. The reduced and sintered samples were characterized by XRD to follow up the crystallinity, total porosity measurement was used to find out the densification properties, the grain structure and morphology were examined by RLM and SEM attached with EDAX. Micro-hardness tester was also used to investigate the influence of sintering conditions on the grain densification. A fundamental study on the kinetics of reduction of mixed nano-sized metal oxides precursor was performed by isothermal and non-isothermal techniques. Both results from isothermal and non-isothermal tests were used to calculate the activation energy which was correlated with macro- and micro-structures to predict the corresponding reduction mechanism. However, the influence of sintering temperature and time on the crystallinity of the produced phases, grain structure, morphology, total porosity, pore-size distribution, bulk and apparent densities, and the hardness of sintered compacts was extensively investigated. The results revealed that the presence of NiO and/or Fe2O3 in the mixed metal oxides precursor was very important to ease the reducibility of WO3 as the metallic phases of Ni and/or Fe act as a catalyst for the reduction of WO3. The rate of reduction proceeds faster in the following order: NiO > Fe2O3 > mixed oxide > WO3. In non-isothermal experiments, it was found that the heating rate has a considerable effect on the reduction of precursor, i.e., the lower the heating rate, the higher the degree of reduction. It might be reported that the use of nano-sized metal oxides particles in the fabrication of heavy tungsten alloys greatly affects the main properties of the produced alloy. With the increase in sintering time, larger sizes of dense grains were developed, and the matrix became denser as a result of sintering and re-crystallization effects. The higher the sintering time, the higher the grain densification and the less pores formed in the matrix. On the other hand, with the increase in the sintering temperature, the grain boundaries were well defined in which the grains were composed of tungsten metal and surrounded by inter-metallics. The higher the temperature, the higher the XRD peak intensities of metallic tungsten and intermetallics as a result of sintering and re-crystallization.

Documenting Territorialidad: an intercultural approach to the provenance of Mapuche land records

Using critical place research and documentary methods, this article examines the Mapuche territorial cause in Chile and exposes the deficiencies of state-produced Mapuche land titles, known as Títulos de Merced, which are required for and (mis)used as evidence by Chile’s Indigenous land restitution program. The Títulos de Merced were granted to Mapuche families during and after the military occupation of Wallmapu (Mapuche territory), as documentation of their relocation to reducciones (reservations) between 1884 and 1929. However, these approximately 3000 titles do not fully represent Mapuche land claims. Instead, they were used by the newly formed Chilean state to reduce Mapuche territory to approximately 5% of its ancestral span, leaving undocumented much of the territories that communities were effectively using before the reduction process––what Mapuche claimants refer to as tierras antiguas or ancestral lands. Despite this, CONADI, the government agency that administers the land program, defines these titles as the primary sources of documentary evidence to prove Mapuche land dispossession. Therefore, not only are the Títulos de Merced not enough, but they negatively impact Mapuche land claims by purposefully reducing, once again, Mapuche ancestral territory, this time discursively. Mapuche claimants are paradoxically forced to validate claims to their ancestral land through documents that were designed to legitimize their dispossession. By examining the insufficiency and inappropriateness of the Títulos de Merced as evidence for Mapuche territorial claims, this paper proposes the intercultural practice of documenting territorialidad—the expression of cultural, economic, and spiritual Mapuche practices over the territory—in addition to colonial demarcations of land, as a form of producing/using evidence for Mapuche land restitution claims. Suggesting the mapu (land/territory) as provenance and territorialidad as evidence, this alternative documentary practice unsettles the Títulos de Merced as the only legitimate form of evidence for Mapuche land claims and theorizes interculturalidad—the recognition of and dialogue between diverse ways of knowing coexisting within the same territory—as a framework for thinking about provenance when working with Indigenous land records.

A bifunctional thiobenzamide additive for improvement of cathode kinetics and anode stability in lithium-sulfur batteries

Lithium-sulfur batteries (LSBs) are considered as the key candidates for the next generation of energy storage devices. However, the practical applications of LSBs are hindered by the slow conversion of sulfur species and the inhomogeneous Li+ precipitation /stripping of lithium anode. Here, we report a bifunctional thiobenzamide electrolyte additive, 4-(trifluoromethyl) thiobenzamide (TFBCA), which synergistically improves cathode redox kinetics and anode stability. Polysulfides (LiPSn) are in-situ transferred to more reactive polysulfide intermediates (T-Sn-T), which significantly improve the liquid–solid reduction process by promoting the deposition dimension of Li2S. A LiF/Li3N-rich solid electrolyte interphase is formed with TFBCA, the uniform lithium deposition is achieved and the growth of lithium dendrites is suppressed. Correspondingly, LSBs with TFBCA show a high capacity (888 mAh·g−1 at 5C) and cycling stability (0.055 % per cycle after 600 cycles at 2C). Even under high sulfur loading (7.1 mg·cm−2) and low E/S ratio of 7, the LSBs also exhibit an areal capacity of 7 mAh·cm−2 after 50 cycles, and an energy density of 314 Wh·kg−1 is achieved for the pouch cell. This work demonstrates an efficient additive strategy through molecular structure design to construct high-performance LSBs.

Unveiling the role of artificial intelligence in tetracycline antibiotics removal using UV/sulfite/phenol advanced reduction process

UV/sulfite-based advanced reduction processes (ARP) have attracted increasing attention due to their high capability for removing a wide range of pollutants. Therefore, developing UV/sulfite ARP systems with assisted Artificial Intelligence (AI) models is considered an efficient strategy for sustainable pollutant removal. The present study delves into modeling and optimizing photodegradation of tetracycline (TC) antibiotics under UV/sulfite/рhenol reԁuсtion рroсess (UV/SPAP) using integrаteԁ Artifiсiаl Neurаl Networks (ANN), Suррort Veсtor Regression (SVR), аnԁ Genetiс Algorithm (GA). The сonсentrаtions of рhenol (X1) аnԁ sulfite (X2), рH (X3), reасtion time (X4), аnԁ TC сonсentrаtion (X5) in our exрerimentаl setuр were varied, аnԁ use the generаteԁ ԁаtа to trаin AI moԁels. The findings revealed that the AI-optimized performance is very effective in predicting and optimizing the removal of TC, thereby providing a sustainable water treatment approach. In general, SVR performed better based on scaling coefficients and ANN using different criteria indicated that X4 and X5 parameters were statistically significant. Oрtimаl rаnges for X1, X2, X3, X4, аnԁ X5 аre ԁetermineԁ to be 6.34, 3, 8.45, 80.13, аnԁ 1, resрeсtively. This аррroасh highlights the imрortаnсe of integrаting AI аnԁ ARP for sustаinаble environmentаl mаnаgement.

Cement modified and copper oxide enriched ferric sludge as oxygen carrier for chemical looping combustion

This study focuses on enhancing the performance of water treatment sludge as an oxygen carrier (OC) for chemical looping combustion (CLC) of municipal solid waste (MSW) syngas. High aluminate cement was introduced to augment the OC’s mechanical strength, concurrently preventing inter-particulate agglomeration, resulting in a commendable and low agglomeration rate of 3.44% after 50 cycles. The inclusion of CuO proves to be instrumental in boosting the OC’s reactivity, mitigating the loss of active components due to the addition of cement support. Notably, FSCuO10 (Ferric sludge with 10% CuO addition) demonstrates over 92% CO efficiency throughout 50 cycles, affirming the success of the dual modification of FS. The investigation also delves into comprehending the reduction process, agglomeration pathways, and the impact of varied CuO percentages has on OC performance. Extensive characterizations were conducted to elucidate OC transformations and their consequential effects on reactivity, physical characteristics, and overall performance. A noteworthy observation includes the outward migration of iron and copper during CLC, contributing to the stabilization of reactivity. In summary, the modifications implemented on FS, yield an improved OC for CLC purposes, maintaining its novelty and cost-effectiveness. The novelty stems from the interactions between CuO and FS, leading to improved reactivity and stability, as well as the extended CLC, which demonstrates the longevity of the OCs. This research contributes to the circularity of waste-derived products by effectively repurposing water treatment sludge and improving sustainable waste management practices.

Production and characterization of nano-magnetic material through different red mud reduction processes

Red mud (RM), is an industrial waste deriving from the production of primary aluminium, with about 200 Mtons generated annually. In this work, the reduction of RM for obtaining magnetic products with particular chemical-physical characteristics has been explored. RM reduction was carried out in a semi-closed reducing environment at a high processing temperature (750–1100 °C) in the presence of carbon-rich ash (CA) resulting from a commercial pyro-gasification plant and by using an H2 atmosphere. All the materials were characterized by elemental analysis, XRD diffraction technique, SEM/EDX microscopy, thermogravimetry and infrared spectroscopy. The materials obtained under the different conditions have in common the presence of small iron-magnetic domains (with different iron oxidation states), in the order of hundreds of nanometres, and by the ferro-magnetic or paramagnetic response to an external magnetic field. In particular, the material pre-treated with HCl (enriched in iron) and reduced with H2 showed very good magnetic responses, more iron in reduced oxidative states showing high ferro-magnetic responses to the external field. The synthesised materials are quite differents each others and appear to have several potential fields of application, as sorbents for specific wastewater pollutants, as materials for CO2 capture, for catalysis and (bio)sensing applications. Nevertheless, the high interconnection between the magnetic and non-magnetic phases limit the direct separation or the iron enrichment. Further efforts should be focused on the functional studies and subsequent LCA and LCC analyses.

Flotation separation of maghara coal in Egypt for the removal of hazardous Cr(VI) from industrial wastewater

ABSTRACT Due to its serious toxicity, wastewater contaminated with hexavalent chromium (Cr(VI)) has become an increasing environmental concern. Herein, a novel flotation separation of maghara coal in Egypt for Cr(VI) removal was proposed to separate coal to three types of maceral group fractions including liptinite, vitrinite, and inertinite via controlling in density as a function in the degree of coalification. The results implied that the activated inertinite macerals (AIM) have the highest carbon and lowest nitrogen levels among the entire maceral groups. The Langmuir isotherm model exhibited a high adsorption capacity of the AIM sample (1226. 21 mg/g) compared to pre-flotation separation sample (877.55 mg/g). Therefore, the flotation separation of maghara coal played a vital role in the Cr(VI) removal. The residuary concentration of Cr(VI) after adsorption onto AIM was close to 0.037 mg L−1 at pH = 2, which satisfies the industrial wastewater discharge standard. In addition, the removal of Cr(VI) onto AIM surface has been demonstrated to be highly effective via the adsorption and reduction process. The oxygen-containing functional groups could strengthen the interaction between Cr(VI) and AIM surface through the reducing reactions. The accelerating effect of organic acids was investigated for the capture of Cr(VI) and the efficiency in the presence of tartaric acid was improved up to 99.96% within 48 h compared to other organic acids. Therefore, this research provides a sophisticated strategy for separating coal to highly efficient adsorbents for wastewater remediation.

Controlled synthesis of tantalum-based solid solution and exploration of electrochemical properties as soluble anode for molten salt electrolysis

Metal oxycarbide solid solution possesses an extensive potential applications due to its remarkable physical features. In this paper, TaCxO1-x solid solution is successively and controllably synthesized by carbothermal reduction of Ta2O5. Based on the thermodynamic calculation, the possible reactions under different conditions in the carbothermal reduction process were analyzed, which provides theoretical guidance for controllable regulation and optimization of carbon thermal reduction process. The effects of carbon content, sintering temperature, and holding time on the synthesis of TaCxO1-x solid solution were investigated and the ideal process parameters for the synthesis of single-phase solid solution were identified. A single-phase solid solution with a carbon‑oxygen ratio close to 1:1 can be created as a soluble anode if the synthesis temperature is 1500 °C, the holding period is 6 h, and the molar ratio of C/Ta is 3.42. Moreover, the process feasibility of preparing metal tantalum by electrolysis of tantalum-based soluble anode is discussed, which provides a new method for metal tantalum preparation.

Recycling of Spent Graphite from Lithium-Ion Batteries for Aqueous Zn Dual-Ion Batteries.

As lithium-ion batteries (LIBs) become more widespread, the number of spent LIBs gradually increases. Until now, recycling of spent LIBs has mainly concentrated on high-value cathodes, but the anode graphite has not yet attracted wide attention. In this work, spent graphite from LIBs was oxidized to graphene oxide and then thermally reduced to reduced graphene oxide (RGO), which serves as the cathode of aqueous Zn dual-ion batteries (ZDIBs). The thermal reduction process enables RGO with a large layer spacing and porous structure, which increase the anion insertion sites and transfer kinetics. As a result, the corresponding battery exhibits a high specific capacity of 96.82 mAh g-1 at 1 A g-1, superior rate capability, and a high capacity retention rate of 80% after 2000 cycles. Moreover, RGO gradually transforms into a long-range disordered structure during the cycling process, which provides more transport routes and active sites for anion insertion and thus leads to the increase of capacity. This work combines the recycling of spent graphite with aqueous ZDIBs, realizing the high-value use of spent graphite.

The portable stochastic sensor as a screening tool for simultaneous determination of HER-1 and CA 125 - a key factor in the rapid recognition of gastric cancer.

The significance of HER-1 and CA 125 lies in their ability to guide cancer diagnosis, treatment, and monitoring, improving personalized care and enhancing prognostic accuracy. The utilization of HER-1 and CA 125 as screening biomarkers for the anticipation of early-stage cancer and monitoring cancer progression is expanding due to the invasive and costly nature of present techniques.In this study, a novel stochastic sensor was developed forthe simultaneous determination of HER-1 and CA 125 in whole blood, saliva, and gastric tumor tissue samples usinga fast, easy, inexpensive, and portable method.The stochastic sensor was prepared by electropolymerization of cysteine on the surface of the Au-TiO2@rGO/SPCE sensor. The Au-TiO2@rGO nanocomposite was synthesized using a simple chemical reduction process. The proposed sensor showed wide linear concentration ranges and very low limits of quantification (LOQ). The concentration ranges were from 3.9 × 10-14 to 3.9 × 10-8µgmL-1, with a LOQ of 3.9 × 10-14µgmL-1 for HER-1. For CA 125, the concentration ranges were from 8.3 × 10-14 to 8.3 × 10-10 U mL-1, with a LOQ of 8.3 × 10-14 U mL-1. Both biomarkers exhibit precise discrimination in different biological samples, with recoveries above 96.78% and RSD values below 0.04%. With a confidence level of 99%, the Student t-test revealed that there is no statistically significant difference between the outcomes obtained by using the poly-Cys/Au-TiO2@rGO/SPCE sensor for screening examinations of biological samples. This was determined because the results were not significantly different from one another.

Self-sulfur doped mesoporous novel carbon electrodes derived from poly-anthraquinone sulfide for high-performance supercapacitors! A comparative study

Carbon materials are suitable electrode candidates in supercapacitors (SCs) because of their availability, well-defined microstructures, and ultrahigh surface areas. Herein, a universal chemical activation method was utilized to obtain activated carbon (C-KOH) from poly-anthraquinone sulfide (PAQS) at 850 °C and reduced activated carbon (C-KOH-H) from C-KOH via a mild hydrogen reduction process at low temperature. The electrochemical performances of the PAQS derived activated carbon electrodes were investigated by assembling electric double-layer capacitors (EDLCs). Electrodes fabricated from C-KOH and C-KOH-H showed 174 and 182.3 F g−1 specific capacitances at 0.5 A g−1 current density, respectively. Whereas their energy densities were 44 and 46 Wh kg−1 at 350 and 423 W kg−1 power densities, respectively. SCs assembled from C-KOH-H showed excellent rate performance, that retained 140 F g−1 even at high current density (20 A g−1), while the one assembled with C-KOH stored 54 F g−1. Furthermore, the C-KOH-H electrode retained 98 % of the initial capacitance at 1 A g−1 over 20,000 continuous cycles. The experimental results revealed that C-KOH-H showed the best electrochemical performance in SCs, which is attributed to the presence of less sulfur and oxygen than C-KOH after the mild reduction. These results prove that PAQS show excellent activation with KOH to produce well-organized porous activated carbons having high specific surface areas, which can be utilized as high-performance electrode materials in SCs.

Relevance of surface characterization of <i>Bambusa vulgaris</i> (l.) leaf extract doped iron nanoparticle

In the present study, green nano scaled zero-valent irons (nZVI) were synthesized from Bambusa vulgaris leaf extract at room temperature. The plant extract was evaluated for the presence of reducing agents (bioactive compounds) phytochemically using standard methods. nZVI was systematically characterized using Scanning Electron Microscopy (SEM), X-Ray Diffraction (XRD), Ultraviolet-Visible (UV-Vis), and Fourier Transform Infra-Red (FT-IR) techniques. The SEM and XRD results showed that after the reduction process for 4 hr at 25oC, the iron powder obtained was a single phase of lamellar or platy α-Fe crystals with the presence of medium nanoparticles (10-100 nm) having crystal size, L ranging from 40-46 nm (42.2 nm) and particle size, D ranging from 53-70 nm (56.1 nm) for both 0.3 M and 0.9 M B. vulgaris-nZVI. It has been demonstrated that B. vulgaris leaf extract was capable of producing iron nanoparticles that shows good stability in solution and under the UV-Visible wavelength, nanoparticles exhibited quite good surface plasmon resonance behavior in the range of 220-740 nm. The FT-1R spectra revealed that the vibrational bands at 3722.76 cm-1 and 3706.4 cm-1 represented the O-H stretching due to the presence of polyphenol as a functional group in addition to tannins, saponins, and others which may be responsible for the eduction of ferrous ion (Fe3+) to zero-valent iron (Feo). This study reveals that B. vulgaris-nZVI possessing short-time synthesis protocol, anisotropism, and eco-benignity could be promising lowcost matrix for remediation (both soil and water), adsorption, catalysis, and other applications.

Enhancement of oxygen flux through Nb-doped La0.4Sr0.6FeO3-δ ceramic hollow fiber membranes by Fe exsolution

In recent years, numerous studies have focused on the use of mixed ionic-electronic conducting oxides for coupled oxygen separation and catalytic reactions in membrane reactors. A promising strategy for the efficient fabrication of oxygen separation membranes involves modification of the membrane surface via exsolved metal nanoparticles decoration. Here, we present a detailed characterization of the structural and transport properties of a novel membrane material La0.4Sr0.6Fe0.95Nb0.05O3−δ (LSFNb5). The exsolution of Fe nanoparticles was observed after heating of LSFNb5 in a reducing atmosphere (5 % Н2/Ar) and was confirmed by X-ray diffraction analysis, Mössbauer spectroscopy, high-resolution transmission electron microscopy and X-ray photoelectron spectroscopy. The formation of Fe nanoparticles on the surface of LSFNb5 hollow fiber membrane in the reduction process leads to the enhancement of oxygen fluxes and reduces the apparent activation energy. Kinetic parameters for oxygen transport through LSFNb5 hollow fiber membrane estimated using two different models, are in good agreement with the experimental results. Furthermore, LSFNb5 hollow fiber membrane demonstrates stable performance both before and after surface treatment.