Mixture Ratio Research Articles

Isotope-dependent site occupation of hydrogen in epitaxial titanium hydride nanofilms.

Hydrogen, the smallest and lightest element, readily permeates a variety of materials and modulates their physical properties. Identification of the hydrogen lattice location and its amount in crystals is key to understanding and controlling the hydrogen-induced properties. Combining nuclear reaction analysis (NRA) with the ion channeling technique, we experimentally determined the locations of H and D in epitaxial nanofilms of titanium hydrides from the analysis of the two-dimensional angular mappings of NRA yields. Here we show that 11 at% of H are located at the octahedral site with the remaining H atoms in the tetrahedral site. Density functional theory calculations revealed that the structures with the partial octahedral site occupation are stabilized by the Fermi level shift and Jahn-Teller effect induced by hydrogen. In contrast, D was found to solely occupy the tetrahedral site owing to the mass effect on the zero-point vibrational energy. These findings suggest that site occupation of hydrogen can be controlled by changing the isotope mixture ratio, which leads to promising manifestation of novel hydrogen-related phenomena.

Performance Evaluation and Optimization of Binder-Toner and Mixing Efficiency Ratios in an E-Waste Toner-Modified Composite Mixture Using Response Surface Methodology

E-waste toner (EWT), which is produced in large quantities by modern industries, has the potential to be utilized as a bitumen modifier to improve engineering properties and save costs. The current study focuses on exploring the optimization of EWT content to identify the most optimal proportions for achieving desirable levels of mechanical properties. This study also examined the effects of E-waste toner contents ranging from 0% to 30% on the fresh consistency of toner-modified and unmodified binder. The study utilized a central composite design (CCD) together with the response surface methodology (RSM) to optimize the mix design variables, specifically the binder-toner ratio (BT) and mixing efficiency ratio (MER). The objective of this study was to examine the combined effects of these variables on the mechanical characteristics of EWT-modified asphalt mixtures. The mechanical responses were obtained through the performance of four responses such as Marshall stability (MS), Marshall flow (MF), indirect tensile strength (ITS), and stiffness tests. The findings suggest that the combined interaction of BT and MER ratios has an impact on their mechanical characteristics. However, the BT ratios had a significant impact on the volumetric attributes compared to MER. The RSM-based prediction models had an R-square over 0.86 across each response. This demonstrates that the inclusion of BT and MER ratios were accountable for a minimum of 86% of the alterations in the mechanical characteristics of EWT-modified asphalt. The multi-objective optimization analysis determined that the optimal proportions for the EWT-modified asphalt, in order to obtain the ideal consistency, were 0.249 ratio of BT and 1.63 ratio of MER with a desirability value of 0.97. Overall, it was found that RSM is a reliable technique for precisely forecasting the mechanical properties of EWT-modified asphalt, including BT and MER ratios.

Study of nifedipine solubility in physical mixtures and solid dispersions

Introduction. Poor aqueous solubility significantly hinders the bioavailability of numerous orally administered drugs. Nifedipine, a widely-used cardiovascular agent, is categorized as practically insoluble according to pharmacopoeias, thus presenting a significant challenge in formulation development. This study investigates the potential of solid dispersion (SD) technology and physical mixtures to improve the dissolution profile of nifedipine.Aim. Development of a technological method for increasing the solubility of nifedipine by developing physical mixtures and SD with the aim of creating a dosage form with improved properties.Materials and methods. Nifedipine, methanol, nifedipine standard samples, potassium dihydrogen phosphate, sodium heptanesulfonate, phosphoric acid (85 %), purified water, and pvp K-30. Solubility studies were performed by HPLC using three objects: nifedipine, a physical mixture (PM), and SD of nifedipine with PVP K-30. The study assessed the effect of different ratios (nifedipine : PVP K-30) in the physical mixture and SD on nifedipine solubility. Fourier transform infrared spectroscopy (IR spectroscopy) and powder X-ray diffractometry were used to characterize the samples.Results and discussion. A notable increase in nifedipine solubility was observed in both PM3 (1 : 3 nifedipine : PVP K-30) and SD3 (1 : 3 nifedipine : PVP K-30). PM3 exhibited a solubility of 9.70 %, while SD3 demonstrated a remarkable enhancement to 32.07 % compared to the pure nifedipine (0.24 %). FTIR analysis did not reveal significant interactions between nifedipine and PVP K-30. PXRD results confirmed the transition of nifedipine from a crystalline to amorphous form within the hydrophilic PVP K-30 matrix, contributing to the observed solubility enhancement.Conclusion. The study highlights the effectiveness of SD technology in significantly improving nifedipine solubility and potential bioavailability. The 134-fold increase in solubility achieved with SD3 at a 1 : 3 ratio demonstrates the significant potential of this approach for enhancing the pharmacokinetic properties of poorly soluble drugs. This research opens up new avenues for developing innovative formulations with improved dissolution characteristics and potentially enhanced therapeutic efficacy.

Change in the Chemical State of Phosphorus Sulfide Molecules Inside Single‐Walled Carbon Nanotubes

This article presents the first experiments on filling single‐walled carbon nanotubes (SWCNTs) with the phosphorus sulfides P4S3 and P4S10 using the ampoule method. Transmission electron microscopy examination reveals the encapsulation of phosphorus and sulfur species inside the cavities of SWCNTs without the formation of any regular structures. X‐ray photoelectron spectroscopy observes different oxidation states of P and S atoms, depending on the P/S ratio in the initial mixture used to fill the nanotubes. The Raman signals associated with the encapsulated species are low in intensity, and the vibrational modes are shifted and broadened as compared to those in crystalline P4S3 and P4S10. The proposed models for the arrangement of sulfur and phosphorus inside SWCNTs suggest the formation of 1D amorphous glassy phosphorus sulfides with stoichiometric ratios close to those of elemental phosphorus and sulfur in the initial mixtures.

Thermophysical Properties of Silicon Oxide Nanoparticles in Water and Ethylene Glycol–Water Dispersions

Measurements of transmission as well as thermophysical properties have been carried out for different concentrations of SiO2 nanoparticles (0, 1, 2, 5, 10, and 20 wt.%) in pure water (W) and ethylene glycol–water mixture (EG/W) in a weight ratio of 25/75, from 298 to 323 K at 100 kPa. In particular, the density, specific heat capacity, and thermal diffusivity are measured by a density meter, differential scanning calorimetry, and the laser flash method. In the case of 20 wt.% SiO2, transmission in the visible range is reduced by 9.3%. Simultaneously, the density rises linearly to 12.3% (in W) and 11.3% (in EG/W). The specific heat capacity decreases to 15.9% (in W) and 17.3% (in EG/W), while the thermal diffusivity rises to 16.4% (in W) and 20.4% (in EG/W). While the density measurements are in very good agreement with the literature, the measured values of the specific heat capacity deviate more than 5%, especially for concentrations below 5 wt.% SiO2. Moreover, it is shown that the thermal conductivity increases less for fluids in small gaps compared to other authors, which could be due to the suppression of the Brownian motion. Based on the measurement results, temperature- and concentration-dependent correlations for the investigated thermophysical properties are developed using two adjustable parameters. In general, these correlations show deviations of less than 4% from the experimental results, which will help to fill the gaps in the variation of experimental results due to size, SiO2 nanofluid production, and different measurement devices, and thus optimize solar thermal applications with SiO2 nanofluid.

Efficient separation of methyl ethyl ketone and water azeotrope using hydrophobic amino acid ester ionic liquids

BackgroundMethyl ethyl ketone (MEK), an essential organic solvent, is commonly produced via the n-butene method, where water emerges as the principal impurity. The conventional distillation processes, which are necessitated by the azeotropic behavior between MEK and water, result in a substantial expenditure of energy. As a result, liquid-liquid extraction represents a promising alternative for energy-efficient separation. MethodsIn this work, three hydrophobic amino acid ester ionic liquids L-phenylalanine ethyl ester bis(trifluoromethylsulfonyl) imide ([Phe][NTf2]), L-leucine ethyl ester bis(trifluoromethylsulfonyl) imide ([Leu][NTf2]) and L-valine ethyl ester bis(trifluoromethylsulfonyl) imide ([Val][NTf2]) were utilized as extractants for separation of the binary azeotrope methyl ethyl ketone and water. The effects of extraction time, extraction temperature, mass ratio of MEK-water mixture to ionic liquid and initial concentration of MEK on extraction efficiency were investigated. Significant findingsThe results demonstrate that the ionic liquid [Phe][NTf2] exhibits superior extraction ability for the separation of the azeotrope methyl ethyl ketone and water. The maximum extraction yield of 99.86 % was achieved with the optimum extraction conditions of extraction time, 10 min, extraction temperature, 293.15 K, mass ratio of mixture to ionic liquid, 1:1 and initial concentration of MEK, 20 %. In addition, the relationship between the structure of ionic liquids and their extraction performance was revealed by quantum chemical calculations of ionic liquids with MEK and water. These ionic liquids were positioned as promising environmentally friendly alternatives to traditional organic solvents for the recovery of MEK from aqueous solutions, providing valuable insights for industrial applications.

A green approach for dyeing cotton fabrics using synthesized reactive disperse dyes and their mixtures under supercritical CO2 medium.

Dyeing natural fabrics using supercritical carbon dioxide is challenging, especially without essential color hues. This work demonstrated that two newly developed reactive disperse dyes with distinct colors and shades were generated, one of which featured from the anthraquinone family and the other yellow, containing a pyrazole moiety. These new dyes and their combinations were used to dye cotton fabric using supercritical carbon dioxide and the highest K/S values were achieved at 8.73 for the mixture of (blue dye: yellow dye 80:20), however the lowest K/S was observed at 7.71 for (blue dye: yellow dye 20:80). The new dyes' chemical compositions were identified using elemental and spectroscopic analyses. The effectiveness of these dyes and their mixtures for cotton dyeing was discussed. The dyed samples were tested for color fastness, and the results indicated that they had excellent color retention and were highly durable in washing. The increasing patterns in both dyeing rate and build-up curves show good compatibility. Furthermore, desirable shades of green can be achieved by mixing blue and yellow dyes at various ratios in supercritical CO2. The compatibility test involves calculating color difference index values for dyed cotton fabrics by utilizing various ratios of a binary mixture of dyes. Furthermore, the dyes under study and dyed samples displayed superior antibacterial properties against gram-positive and gram-negative bacteria compared to certain antibiotics used as a control. These results aligned with the quality and eco-friendly standards required by the industry without the use of water.

Coupling thermodynamic modelling with experimental study to reveal the evolutionary relationship of pore solutions, products, and compressive strength for lunar regolith simulant geopolymers

Alkali-activation is a highly promising approach for the in situ resource utilisation (ISRU) of lunar regoliths. However, the considerable variation in the composition of lunar regolith simulants can complicate the optimal design of geopolymer mixture ratios, necessitating an in-depth analysis of composition–performance correlations. This study proposes a calculation method that couples thermodynamic modelling with an experimental study to reveal the evolutionary relationship between the pore solution, product formation, and compressive strength. The results indicate that the modulus and dosage of the alkali activator can substantially change the relative content of reactive elements in the pore solution and affect the product type and content. Among these, [Si] and [Al] in the pore solution and gel production are key factors affecting the compressive strength of geopolymers. Understanding these composition–performance relationships is critical for offering essential guidance for performance-based, on-demand material design and optimisation.

High-energy Mn2V2O7//C asymmetric supercapacitors in aqueous/organic hybrid electrolytes

The demand for advanced energy storage devices, such as high-energy density supercapacitors, has spurred efforts to develop new environmentally friendly and efficient electrode materials and electrolyte solutions for sustainable development. A prominent strategy is the fabrication of high-voltage and energy-density asymmetric supercapacitors (AS). In this study, dimanganese divanadate (Mn2V2O7, MVO) particles were synthesized via a hydrothermal process and used as pseudocapacitive electrodes for AS. The pseudocapacitive MVO electrode offered synergistic advantages of reversible surface or near-surface Faradaic reactions for charge storage. Another approach to address the challenges of limited energy density in supercapacitors was modifying the electrolyte solution to widen the operating voltage window and increase energy density. A hybrid electrolyte solution of 5 M sodium perchlorate (NaClO4) in a mixture of (2:1) volume ratio of acetonitrile (AN) and water (H2O) was introduced to expand the voltage window in the AS. The fabricated AS with MVO as a pseudocapacitive electrode and activated carbon as a double-layer capacitive electrode operated in a voltage window > 2.0 V with the hybrid electrolyte. The AS device exhibited a capacitance of 156.9 F g−1 at 0.1 A g−1 and a high energy density of 87.2 Wh kg−1, surpassing the carbon-based symmetric supercapacitor (58.9 Wh kg−1). Furthermore, the pseudocapacitive supercapacitor showed exceptional long-term stability over 50,000 cycles. Structural and surface characterization of the MVO electrode after CV testing validated that the charge storage mechanism in Mn2V2O7//C was a surface-controlled process. The performance of the AS pouch cell revealed the great promise of the pseudocapacitive electrode in practical applications.

Physicochemical properties of lard oil and rubber seed oil blends and their comprehensive characterization

This research investigates the potential of blending complementary lard oil with rubber seed oil as feedstock for biodiesel production. Rubber seed oil, obtained through hexane extraction using the Soxhlet method, contains the major fatty acids of oleic acid (C18:1), palmitic acid (C16:0), linoleic acid (C18:2), and stearic acid (C18:0), while rubber seed oil primarily consists of linoleic acid (C18:2), oleic acid (C18:1), linolenic acid (C18:3), palmitic acid (C16:0), and stearic acid (C18:0). Th least acid value of lard oil (0.55 mg KOH/g) can benefit of reducing soap formation of rubber seed oil during transesterification process in biodiesel production due to its substantial-high acid value (16.28 mg KOH·g–1). Blending at ratios below 80:20 v/v produced biodiesel exceeding 85%, utilizing CaO as a catalyst. Lard oil demonstrated a higher reaction rate constant (11.88×10–3 min–1) than rubber seed oil (2.11×10–3 min–1), indicating a significant difference in performance. High acid value and free fatty acids in rubber seed oil correlated with lower reaction rates. Maintaining a mixture ratio below 80:20 v/v optimized reaction rates during biodiesel production. Biodiesel obtained from blends below 80:20 v/v met ASTM D6751 and EN 14214 standards, demonstrating suitability for bio-auto fuel. The drawbacks of using rubber seed oil as a raw material for biodiesel production are overcome by blending with lard oil, giving rise to expanding renewable energy options for rural communities, community enterprises, and large-scale biodiesel production.

Experimental research on the flexural properties and pore structure characteristics of engineered geopolymer composites prepared by calcined natural clay

The synthesis of high ductility geopolymer composites using excavated natural clay is an economical and environmentally friendly method to realize the utilization of excavated natural clay. This paper presents an experimental research on the flexural properties and pore structure characteristics of engineered geopolymer composites (EGC) prepared by calcined natural clay. The EGC with different slag and fiber contents were prepared and the four-point bending tests were conducted on the EGC. The effect of slag and fiber content on the flexural strength, flexural deflection and flexural toughness were discussed. The microscopic pore structure characteristics of EGC were further analyzed. The optimal mixture ratio of calcined clay-based EGC with the highest flexural toughness was proposed. The results show that fiber can significantly enhance the flexural properties and cracking control ability of EGC. The ultimate flexural strength, flexural deflection, flexural strengthening index and flexural toughness of EGC all increase with increasing fiber content. The results also show the addition of 10.0% slag can increase the flexural strength and flexural toughness, while excessive slag content reduces the flexural properties. The EGC with 10.0% slag content and 2.5% fiber content exhibits excellent flexural properties and cracking control ability. The ultimate flexural strength and flexural toughness index reach 9.75 MPa and 486.11, showing the highest flexural toughness.

The Properties of Thin Films Based on Chitosan/Konjac Glucomannan Blends.

In this work, blend films were prepared by blending 2% chitosan (CS) and 0.5% konjac glucomannan (KGM) solutions. Five ratios of the blend mixture were implemented (95:5, 80:20, 50:50, 20:80, and 5:95), and a pure CS film and a pure KGM film were also obtained. All the polymeric films were evaluated using FTIR spectroscopy, mechanical testing, SEM and AFM imaging, thermogravimetric analyses, swelling and degradation analyses, and contact angle measurements. The CS/KGM blends were assessed for their miscibility. Additionally, the blend films' properties were evaluated after six months of storage. The proposed blends had good miscibility in a full range of composition proportions. The blend samples, compared to the pure CS film, indicated better structural integrity. The surface structure of the blend films was rather uniform and smooth. The sample CS/KGM 20:80 had the highest roughness value (Rq = 12.60 nm). The KGM addition increased the thermal stability of films. The blend sample CS/KGM 5:95 exhibited the greatest swelling ability, reaching a swelling degree of 946% in the first fifteen minutes of the analysis. Furthermore, the addition of KGM to CS improved the wettability of the film samples. As a result of their good mechanical properties, surface characteristics, and miscibility, the proposed CS/KGM blends are promising materials for topical biomedical and cosmetic applications.

Dispersionless Flat Mode and Vibrational Anomaly in Active Brownian Vibrators Induced by Stringlike Dynamical Defects.

In recent years, active Brownian particles have emerged as a prominent model system for comprehending the behaviors of active matter, wherein particles demonstrate self-propelled motion by harnessing energy from the surrounding environment. A fundamental objective of studying active matter is to elucidate the physical mechanisms underlying its collective behaviors. Drawing inspiration from advancements in molecular glasses, our study unveils a low-energy "flat mode" within the transverse spectrum of active Brownian vibrators-a nearly two-dimensional, bidisperse granular assembly. We demonstrate that this collective excitation induces an anomalous excess in the vibrational density of states (VDOS) beyond the phononic Debye contribution. We characterize the properties of this flat mode by exploring the parameter space of our experimental system and tuning the packing fraction, the vibrational frequency, the particle size ratio, and the mixture ratio. Additionally, we establish through empirical evidence that stringlike dynamical defects, discerned via the spatial distribution of each particle's contribution to the reduced transverse VDOS, serve as the microscopic origin of the flat mode and its associated anomalies.

Studying of Mechanical Behavior of Waste Materials Modified Cement Mortar

Large-scale environmental problems have been triggered by ceramic tiles from demolished buildings and animal bone waste. Therefore, optimizing their potential for reuse and recycling is an important goal of sustainable solid waste management. The primary objective of this study is to evaluate the feasibility of partial replacement of the fine aggregates in cement mortar with a combination of natural animal bone powder and industrial waste materials which is wall tiles ceramic powder. This study measures thermal and mechanical characteristics. Recycling construction waste is one of many ways to deny waste material from entering landfills and create new eco-friendly material that reduces energy consumption in buildings. Modified mortar cement specimens with 5% up to 25% mixtures were combined using a 1:3 ratio and a 0.5 W/C ratio to see how the ratios would affect the material’s properties. The addition of a superplasticizer boosted the cement mortar’s workability and compressive strength. The compressive strength, flexural strength, density, and thermal conductivity were evaluated for each mortar mixture ratio. Results showed that compared to regular cement mortar, cement mortar combined with 20% bone and ceramic powder wastes reached the optimal replacement percentage. Compressive strength increased by 54% and flexural strength by about 67%. At the 28-day mark, thermal insulation was lowered by 25%.It is concluded from this study that it is possible to use bone waste as a natural material with ceramic waste as an industrial material to modify the insulation and mechanical properties of cement mortar.

Internal validation of the Precision ID GlobalFiler NGS STR panel v2 kit with locus-specific analytical threshold, and with special regard to mixtures and low template DNA detection

We performed an internal laboratory validation of the Precision ID GlobalFiler NGS STR panel v2 kit to assist the introduction of the technology into the routine forensic casework practice. The study was designed and evaluated based not only on the key validation standards like sensitivity, stability, reproducibility, repeatability, mixture, and concordance, but we also tested the effect of reduced input DNA, we measured and applied locus-specific analytical threshold values, tested two different PCR cycle conditions, sequence artifacts and stutters were also analysed. During the study we also tested the new method on real casework samples. The sensitivity study confirmed that adding 500 pg template DNA for library preparation can be optimal at base PCR cycle number (that was 24), because the measured average heterozygote balance was not lower than 0.82, and each allele was detected above the analytical threshold. However, contrary to previous communications, increasing the PCR cycle numbers up to 28 has not resulted the significant elevation of the heterozygote imbalance. According to our results, raised PCR cycle condition (i.e. 28) is appropriate at or below 150 pg total input DNA. For most loci, the calculated AT was lower than the manufacturer’s recommended. Applying the newly established ATs with raised PCR cycle conditions the allele detection sensitivity and reliability increased. We observed allele dropouts only at the 15 pg template DNA experiments with 5 % frequency, that is better to previously published studies. This result indicates that this low amount of DNA (i.e. 15 pg) could be a minimum limit of template input for a potentially successful analysis. In the mixture study the minor contributor could be detected up to 1:19 mixture ratio. We detected minor alleles in all measurements and concentrations above the threshold if the template DNA were fixed and only SNP differences were observed between the same alleles of the contributors. To test concordance between the new method and traditional STR genotyping we analysed 58 Hungarian individual samples in parallel. Nearby the detected 248 different length-based alleles on the 31 loci in the sample pool we revealed additional 75 sequence variant alleles, that represent an approximately 23 % increase in the total number of observed alleles. The casework study confirmed that the Precision ID GlobalFiler NGS STR panel v2 kit is effective even in genotyping degraded samples with extremely low levels of DNA, if we apply elevated cycle number for library preparation and use locus-specific analytical thresholds.

Evaluation of the synergic effect of amino acids for CO2 hydrate formation and dissociation

Gas hydrate formation is a very challenging problem in the oil and gas industry. The chemical inhibition method is the best practicable hydrate mitigation method by injecting hydrate inhibitors such as Thermodynamic Hydrate Inhibitors (THIs) and Kinetic Hydrate Inhibitors (KHIs) into the pipeline. However, the hydrate inhibitors' biodegradability and limited data on dual functional inhibitor mixtures raise concerns in this study. This study aims to investigate and compare thermodynamic and kinetic inhibition on CO2 hydrate by using biodegradable amino acid inhibitor mixtures of Glycine and Alanine. In this study, the inhibitor mixtures were prepared by mixing Glycine and Alanine in 3 different mixture ratios, followed by the Thermodynamic and Kinetic inhibition tests. Thermodynamic Inhibition Test was conducted by using 10 wt% of inhibitor mixtures in a CO2-water system under pressure of 4.0, 3.5, 3.0 and 2.5 MPa, while Kinetic Inhibition Test was carried out by using 1 wt% of the sample in the CO2-water system at a constant pressure of 4.0 MPa and temperatures at 274.15K. The analysis methods for the Thermodynamic Inhibition Test were Hydrate Liquid-Vapor Equilibrium (HLVE) Curve, Average Depression Temperature and Molar Dissociation Enthalpy, while the Induction Time method, the number of CO2 moles consumed, the formation rate of CO2 gas hydrate and RIP were used in the Kinetic Inhibition Test. In this study, all inhibitor mixtures exhibit dual functional inhibition on the CO2 hydrate. For THI, 50% Gly: 50% Ala shows the best thermodynamic inhibition strength with an average depression temperature of 2.42 K. All the inhibitor mixtures for THI have the dissociation enthalpies within the CO2 hydrate enthalpy range, which show that the inhibition is due to the influence on the water molecules’ interaction only. For KHI, 75% Gly: 25% Ala shows the highest kinetic inhibition strength on CO2 formation with the longest induction time of 115.2 min and the highest RIP of 0.40. In the KHI experiment, there is a drop in the CO2 uptake capacity with the presence of inhibitors used, where the highest difference of CO2 moles consumed is 0.0057 mol. A synergistic effect of inhibitor mixtures was observed in this study on 50% Gly: 50% Ala for THI and 75% Gly: 25% Ala for KHI. However, the “degradation” effect was also exhibited on 75% Gly: 25% Ala and 25% Gly: 75% Ala for THI and 50% Gly: 50% Ala and 25% Gly: 75% Ala for KHI, where the performance of the inhibitor mixtures is poorer than the concentrated amino acids. The “degradation” effect of the inhibitor mixtures at certain ratios was not covered in this study and it requires a further understanding of the chemistry behind the inhibition mechanism.

Optimization of mixture ratios of raw materials in thermoplastic hybrid composites based on particle swarm optimization algorithm

Optimization of mixture ratios of raw materials in thermoplastic hybrid composites based on particle swarm optimization algorithm

Spark ignition and stable flame of premixed methanol-ammonia gaseous jet at atmospheric surrounding

Ammonia, regarded as a zero-carbon fuel, presents significant challenges due to its notable combustion and chemical inertness. To mitigate these challenges, blending liquid ammonia with carbon-neutral methanol offers a promising avenue for creating an innovative, stable, and large-scale producible carbon-neutral fuel. This study investigates the impacts of xCH3OH (methanol mole ratio in methanol-ammonia mixture) and v (mean jet velocity at nozzle outlet) on forming stable flames of a premixed methanol-ammonia argon-oxygen (MA-AO) gaseous jet in the atmospheric surrounding. Results indicate that the pure ammonia argon-oxygen (A-AO) mixture can be ignited by an electrical spark with the energy of about 52.1 mJ, but it cannot grow to be a stable jet flame although the fire nucleus can form. Blending methanol is very helpful in forming a stable jet flame of the MA-AO mixture. When xCH3OH is lower than 49% at λ = 1.0, only the fire nucleus could be formed without a stable jet flame. When xCH3OH is more than 49%, there is a certain mean jet velocity range for different xCH3OH to form a stable flame. At the low-velocity limit, the flame would be quenching. While the flame would be blown off at the high-velocity limit. The velocity limits of quenching and blow-off become higher with higher xCH3OH, and the blow-off velocity limit increases more evident.

The effect of variations in cold plasma conditions on the detoxification of Aflatoxin M1 and degradation products

The aim of this study was to explore the chemical reactive species of different operating gases, and their effect on the degradation of aflatoxin M1 (AFM1) by cold plasma by measuring the reactive species concentration. Helium, at 80, 90 or 95%, was used mixed with oxygen, nitrogen and air. The efficacy of cold plasma on aflatoxin M1 (AFM1) reduction was improved when decreasing the ratio of helium in the gas mixture. The ratio of the gas mixtures changed the cold plasma chemistry believed to be due to the differences in the concentrations of the reactive species. The degradation products of AFM1 after cold plasma treatment using a helium/air gas mixture and the degradation pathway were identified by LCMS. AFM1 was oxidised by reactive species in the cold plasma to produce degradant products with, theoretically, lower toxicity than AFM1.

Carbons prepared by microwave co-pyrolysis of waste scrap tyres and corn cob: Effect of cation size and charge on xylene adsorption

Carbons prepared by pyrolysis of waste corn cobs or scrap tyres using different microwave power (200, 400, 600 W) are compared with carbons prepared by co-pyrolysis of corn:tyre mixtures in various mass ratios without/with activator (KOH, ZnCl2, K2CO3, NaOH in solid or liquid phase). Activation and co-pyrolysis of corn:tyre mixture was proved to be advantageous, prepared activated carbons showed enhanced xylene adsorption compared to non-activated. Activated carbons prepared from corn:tyre mixture at mass ratio of 4:1 and using ZnCl2 in liquid and ZnCl2 and K2CO3 in solid phase showed the highest adsorption capacities (∼171, 139 and 104 mgxylene·g−1, respectively) despite the opposite trend in their microporosity. Molecular modeling proved a preferential interaction of xylene with activated carbons porous structure through Zn2+, K+ and Na+ ions. The smallest cation with the highest positive charge, Zn2+, interacts the most strongly with xylene. The strength of cation-xylene interaction decreases as follows: Zn2+ > Na+ > K+. As the strongest were proved xylene interactions with Pore (5.2 Å)_Zn2+ > Pore (8.5 Å)_Zn2+ > Surface_Zn2+ > Pore (5.2 Å)_Na+ ∼ Pore (5.2 Å)_K+, which explains the highest adsorption capacities of ZnCl2-activated carbons despite of their lower microporosity compared to carbon activated by using K2CO3(s).