Initial Mixture Research Articles

A Screening Approach to Assess the Impact of Various Commercial Sources of Crude Marine λ-Carrageenan on the Production of Oligosaccharides with Anti-heparanase and Anti-migratory Activities.

Oligosaccharides derived from λ-carrageenan (λ-COs) are gaining interest in the cancer field. They have been recently reported to regulate heparanase (HPSE) activity, a protumor enzyme involved in cancer cell migration and invasion, making them very promising molecules for new therapeutic applications. However, one of the specific features of commercial λ-carrageenan (λ-CAR) is that they are heterogeneous mixtures of different CAR families, and are named according to the thickening-purpose final-product viscosity which does not reflect the real composition. Consequently, this can limit their use in a clinical applications. To address this issue, six commercial λ-CARs were compared and differences in their physiochemical properties were analyzed and shown. Then, a H2O2-assisted depolymerization was applied to each commercial source, and number- and weight-averaged molar masses (Mn and Mw) and sulfation degree (DS) of the λ-COs produced over time were determined. By adjusting the depolymerization time for each product, almost comparable λ-CO formulations could be obtained in terms of molar masses and DS, which ranged within previously reported values suitable for antitumor properties. However, when the anti-HPSE activity of these new λ-COs was screened, small changes that could not be attributed only to their small length or DS changes between them were found, suggesting a role of other features, such as differences in the initial mixture composition. Further structural MS and NMR analysis revealed qualitative and semi-quantitative differences between the molecular species, especially in the proportion of the anti-HPSE λ-type, other CARs types and adjuvants, and it also showed that H2O2-based hydrolysis induced sugar degradation. Finally, when the effects of λ-COs were assessed in an in vitro migration cell-based model, they seemed more related to the proportion of other CAR types in the formulation than to their λ-type-dependent anti-HPSE activity.

Crystal growth of fluorine-doped tin oxide structures with extraordinary morphology by the hydrothermal method and their electrical conductivity

In this work, fluorine-doped tin oxide (FTO) crystal structures with different morphology and the phase composition were synthesized by the hydrothermal method. It was shown that the controlled addition of NH4F to the initial solution leads to a change in the pH of the reaction mixture. Varying the pH of the initial mixture results in a change in the shape of growing crystals from a flower-like to a prismatic and phase transformation of the resulting crystal structures. Flower-like FTO structures obtained at a mass ratio of F/SnO2 = 0.05 show the highest conductivity in the synthesized series. A detailed microstructural analysis indicates that these structured particles consist of primary nanocrystals that are misoriented and have different preferential growth directions. It is assumed that an enhancement in the conductivity can be due to the synergistic effect of defects formed during the spontaneous growth of FTO nanocrystals under hydrothermal conditions and their local interaction.

Non-dominated Sorting-Based Strategy for Optimizing the Mixture of Initiators in Polyethylene Reactor

Non-dominated Sorting-Based Strategy for Optimizing the Mixture of Initiators in Polyethylene Reactor

Dry Electrode Manufacturing in a Calender: The Role of Powder Premixing for Electrode Quality and Electrochemical Performance

The dry manufacturing of battery electrodes has the potential to significantly reduce costs and the environmental impact of battery production but deteriorates the electrode quality due to drawbacks in the processability of the materials. By varying the mixing intensity of the powder mixtures, this work investigates the impact of blend homogeneity on the flow properties and the processability of the dry mixtures. Furthermore, the electrochemical performance of dry laminated electrodes made of LiNi0.6Mn0.2Co0.2O2 is investigated with respect to their initial mixture homogeneities and compared to slurry-based electrodes. An improvement of the powder flowability is observed for mixtures with a homogeneously distributed PVDF binder, which acts as a temporary lubricant in dry electrode manufacturing due to its ability to shear, resulting also in filament formation. Capacity and rate performance of electrodes made of homogeneous mixtures are the highest with 169 mAh/g at C/20 and 70 mAh/g at 3C compared to 169 and 49 mAh/g for the slurry-based electrodes, respectively. Cyclic voltammetry indicates lower overpotentials for incompletely homogenized electrodes due to the existence of carbon black aggregates that establish better long-range conductivity. Overall, electrodes from highly homogenized powders show the best electrochemical performance in terms of C-rate capability due to their favorable electrode thickness and porosity resulting from better processability in combination with a sufficiently distributed carbon binder domain.

Modes of interaction of counterflow flames in diluted methane–oxygen mixtures in a closed reactor

The features of the interaction of counterflow flames in diluted methane–oxygen mixtures at a total pressure of up to 200 Torr in a closed reactor were established. It was found that in the mode of interaction of flames propagating in hot reaction products, two-dimensional flame vortices arise due to density stratification; flames, propagating through the initial mixture, interact with the formation of only three-dimensional structures.

Investigation of the conditions for the formation of the α<sub>2</sub>-phase in mechanocomposites of the Ti–Al system by synchrotron radiation methods

Synchrotron studies of the features of the dynamics of phase formation in a mechanically activated 3Ti + Al powder mixture during the implementation of high-temperature synthesis under conditions of volumetric ignition by induction heating are carried out. The effect of the time of preliminary mechanical activation treatment of the initial mixture (1, 3, 7 minutes) on the macrokinetic parameters of synthesis was experimentally investigated.

Estimation of physico-chemical parameters of different combinations of buffalo dung with cane sugar bagasse by Vermic activity of earthworm Lampito mauritii

Overpopulation, pollution, industrialization, and urbanization are the main contributors to environmental deterioration and the production of solid waste. There are many ways to reduce the amount of organic waste that is disposed of in landfills. This covers vermicomposting, recycling, and composting of organic materials. With the aid of earthworms, vermicomposting is one of the most effective, affordable, and environmentally sustainable ways to turn organic wastes into high-quality manure. This study is aimed to investigate the physico-chemical alterations of sugarcane bagasse mixed with various combinations of buffalo dung following the processing of the earthworm Lampito mauritii. After vermic activity of Lampito mauritii, different combinations of sugarcane bagasse combined with buffalo dung showed a substantial decline in pH, EC, TOC, and C/N ratio and a significant rise in TKN, TK, TAP, and TCa when compared to the initial feed mixture. There was significant increase in total kjeldhal nitrogen (TKN) 46.25% in SCB+BD (1:1), total avilable phosphorus (TAP) 52.63% in SCB+BD (2:1), total potassium (TK) 35.13% in SCB+BD (1:1), total calcium (TCa) 52 % in BD and significant decreased in C:N ratio 69.74% in SCB+BD (1:1), total organic carbon (TOC) 54.82% in BD, electrical conductivity (EC) 54.16% in BD of final vermicompost with respect to initial feed mixture. The pH of initial feed mixture in all the combination tends to decrease. According to the findings, Lampito mauritii speed up the mineralization process and transformed manures into castings with increased nutritional content. These composts are suitable for use in agricultural fields since they have a low C: N ratio and high nutritional content, which will improve crop output.

Optical measurements of two cylindrical and conical heavy-duty diesel injector nozzels – A comparison of reference diesel, HVO, and RME fuels

In the present work, a constant volume/constant pressure combustion chamber was utilized to measure the major parameters of vapour/liquid phases and combustion of fuel spray introduced by two heavy-duty, large-diameter diesel injectors. A conical nozzle (K factor 4) with a 300 µm outlet diameter and a 1300 µm length and a cylindrical nozzle (K factor 0) with a 300 µm outlet diameter and a 650 µm length display notably distinct impacts on the formation of the mixture, the air entrainment process, and the combustion behaviour. Several parameters, including jet and liquid spray penetration lengths, jet cone angle, and jet projected area are combined to describe spray characteristics in an inert background gas, and ignition incidence, flame lift-off length, and soot appearance time parameters are calculated to explain the combustion trend of the nozzles in a reactive gas background. These observations were conducted using four distinct optical techniques, two of Schlieren and Mie-Scattering for inert condition, and two of OH* Chemiluminescence and Natural Flame Luminosity for reactive condition. This study collects a wide variety of boundary conditions, comprising ambient pressure/temperature and fuel rail pressure, with diverse fuels, including reference diesel, HVO, and RME fuels.The findings are categorized by the jet and liquid spray behaviours in the first part, demonstrating that the jet cone angle is an injector geometry-based parameter and that the cylindrical nozzle has a larger cone angle and a shorter liquid spray length. Three distinct scenarios of the computed air-to-fuel mass ratio at the same axial positions, time steps, and injected fuel mass indicate a marginally higher air entrainment in the cylindrical nozzle and, presumably, a faster and better mixture formation. The thorough examination of the combustion characteristics indicates that a quicker formation of the initial stoichiometric region in the cylindrical nozzle results in a shorter ignition delay at most experimental locations, which ultimately results in a faster soot initiation. However, depending on the flame lift-off length and the boundary conditions, the interval between ignition and the development of soot varies considerably. Finally, it is demonstrated that, with the exception of fuel pressure variation, the flame lift-off length, which is crucial in providing the initial mixture formation prior to combustion occurrence, follows the ignition delay trend and exhibits a shorter length with a shorter ignition delay.

Numerical simulation on transport behavior of gradated coarse particles in deep-sea vertical pipe transportation

Flow pattern and hydrodynamic characteristics of coarse particles in deep-sea hydraulic lifting pipes are simulated using a numerical approach developed by combining the computational fluid dynamics method with a discrete element method in the Euler–Lagrange framework. This paper examines the effects of feed concentration, two-phase flow initial mixture velocity, and particle gradation on the dynamic characteristics of particles and flow pattern in the pipe by validating the rationality of numerical simulation. The results demonstrate that particles are distributed from the pipe center to the pipe wall, while the lift force causes more particles to be distributed in the pipe center. Moreover, greater inertia makes large particles more concentrated in the center. Particle-induced turbulence modifies the lift force and causes particles to move from the pipe center to its wall. Due to the increasing trend of lift force, particles gather toward the center of the pipe at an increasing pace as the initial velocity increases. The greater the feed concentration, the more particles disperse toward the pipe wall due to the violent momentum exchange caused by the high concentration and the significantly altered lift force caused by the high turbulent kinetic energy resulting from a high concentration. From the particle gradation 1:1:1 to 1:6:1, the pressure drop decreases gradually as the reduction in small particles decreases the number of particles near the wall, and the frictional energy loss between the particles and the pipe wall decreases.

Decomposition of methanol to syngas on supported Pt-containing catalysts

Properties of supported Pt-containing granular (Pt/Ce0.75Zr0.25O2–δ) and monolithic structured (Pt/Ce0.75Zr0.25O2–δ /η-Al2O3 /FeCrAl) catalysts were studied in the methanol decomposition to syngas for feeding solid oxide fuel cells (SOFC). The application of the monolithic structured catalyst in the methanol decomposition reaction was shown to be promising. The addition of a small oxygen amount to the initial mixture was found to prevent the formation of carbon, thus enhancing the stability of catalyst operation. The proposed monolithic structured catalyst 0.15 wt.% Pt/8 wt.% Ce0.75Zr0.25O2–δ /6 wt.% η-Al2O3 /FeCrAl at atmospheric pressure, temperature of ca. 400 °C, feed rate of the reaction mixture 5.6 L/(gcat·h) and volumetric ratio СН3ОН/air = 1 can provide the complete conversion of methanol to syngas with the total content of H2 and СО of ca. 64 vol.% and the syngas output of ca. 6.7 L(Н2 + СО)/(gcat· h).

Sub-micron sized hierarchical porous ZSM-5 particles with controllable mesoporous structures by changing the alkalinity in the synthesis using NaOH

This work reports that sub-micron sized hierarchical porous ZSM-5 particles with controllable mesoporous structures can be facilely synthesized in a seed-assisted system without using any secondary templates or organic additives. The results showed that typical samples so-obtained display relative uniform ellipsoidal sub-micron sized particles consisting of loosely packed primary nanocrystals. The mesoporous structures of ZSM-5 zeolite particles can be effectively introduced and adjusted by solely changing the quantity of NaOH in the initial synthesis mixture. The NaOH dosages significantly affect not only hierarchical mesoporosity but also the ratio of Si/Al and thus acidity of the final ZSM-5 product. Moreover, the effect of synthesis hydrothermal procedure was also investigated. The typical sample Z5-0.12 possesses high crystallinity, BET surface area, well-developed mesoporosity and improved catalytic performance in LDPE cracking. This approach constitutes a facile and cost-effective pathway to prepare sub-micron sized hierarchical porous ZSM-5 particles and might promote their application in industry.

SHS of cast materials in the Mo-Al-C system

Materials based on molybdenum-aluminium-carbon compounds have a considerable potential for use under intense wear conditions at elevated temperatures. This paper presents the experimental results of self-propagating high-temperature synthesis of compounds within the Mo-Al-C system. By combining two processes: SHS of the elements and SHS-metallurgy, cast materials containing the Mo3Al2C, Mo2C, Mo3Al, and Mo3Al8 phases were obtained. The experiments used mixtures with compositions calculated according to the ratio (1 - α)(3MoO3-8Al-C)/α(3Mo-2Al-C), where a varied in the range from 0 to 1. The synthesis was carried out in a laboratory reactor of 3 L volume at an initial argon pressure of 5 MPa. The mass of the initial mixtures in all experiments was 20 g. The process of combustion was initiated by a 0.5 mm diameter molybdenum wire spiral by applying 28 V voltage to it. The resulting end products were studied by X-ray diffraction and local microstructural analysis. A significant influence of the ratio of the initial reagents on the synthesis parameters, phase composition, and microstructure of the target products was established. Introduction into the high-exothermic mixture 3MoO3-8Al-C inert “cold” mixture 3Mo-2Al-C leads to an increase in the content of carbide phases in the ingots. The possibility of obtaining cast materials based on the triple phase Mo3Al2C, the maximum content of which is 87 wt. % at the content of the “cold” mixture in the charge α = 0.4 is shown. The presence of secondary phases of molybdenum carbide (Mo2C) and molybdenum aluminides (Mo3Al8 , Mo3Al) in the final products is due to a change in the composition of the initial mixture caused by the ejection of components during combustion and insufficient existence time of the melt formed in the combustion wave.

Physicochemical and sensory characteristics of extrudates from rice enriched with pumpkin

The purpose of this work was to study the effect of pumpkin flour (10% and 20%), moisture content of initial mixture (14% and 20%) and working screw speed (180 min-1 and 220 min-1) on the physicochemical (expansion, density, hardness, colour) and sensory characteristics of rice extrudates enriched with pumpkin produced on a single screw extruder. The chemical composition before and after extrusion was also determined. The ash, lipids, reducing sugars, total sugars and total protein remained unchanged before and after extrusion while the carotenoids decreased after extrusion. The increase in the pumpkin flour led to a decrease in the expansion and lightness, and an increase in the density, hardness and redness of extrudates. The effect of the moisture content was inversely proportional on the expansion and redness, while it was directly proportional on the density, hardness and lightness. The screw speed increased the expansion, hardness and lightness of the extrudates, decreased the redness and had no significant effect on the density. The highest sensory score was achieved at a moisture content 14%, pumpkin flour 10% and screw speed 220 min-1. The moisture content had the most significant effect on the characteristics of the extrudates.

Formation of products upon ignition, combustion and melting of mixtures of high-entropy alloy FeNiCoCrCu with titanium and carbon

The dependence of the ignition temperature, combustion rate and composition of the resulting products on the concentration of Ti + C in mixtures with powder of a high-entropy alloy (HEA) FeNiCoCrCu and the initial mixture of metals forming it (MIX) has been studied. HEA was obtained by mechanical activation (MA) of a mixture of metal powders in argon. At the melting temperature, the high-entropy FeNiCoCrCu alloy decomposes into several phases, but the basis of the HEA alloy, as well as the alloy obtained by melting and crystallizing MIX, is a 5-component phase with an average formula Cu1.2Fe1.4Ni1.4Co1.4Cr. In addition, 5, 4, and 3-component phases with averaged formulas Cu2Ni2Co2Fe2Cr, Cu3Ni3Co2.9Fe2.5Cr, Cu4.8Ni4.5Co4.6Fe4.2Cr, Cu40Fe2Ni4Co2C, Cr12.5Fe3.2Co2.6Ni and Co3.2 Fe3,5 Cr are present in small amounts in the binder. Experiments on the ignition and combustion of mixtures of MIX and HEA with Ti + C were carried out in argon at atmospheric pressure. The combustion rate, ignition temperature, and maximum temperature reached in the thermal explosion of MIX and HEA mixtures with Ti + C increase with increasing Ti + C concentration. Due to the low exothermicity of the mixtures, the experiments were carried out at an initial temperature of 500 °С. At this initial temperature, the combustion limit of the samples occurs when the Ti + C concentration in the HEA and MIX mixtures is less than 30 %. Based on the results of scanning electron microscopy, the volume concentration of the number of titanium carbide (TiC) particles in molten samples was calculated. In an alloy with a HEA binder, the number of TiC particles per unit volume is 1.5-3.0 times greater than in an alloy with a MIX binder, and their size is correspondingly smaller. With an increase in the concentration of Ti + C from 30 to 40 % in a mixture with HEA, the number of TiC particles per unit volume decreases. In a mixture with MIX, the number of TiC particles per unit volume passes through a minimum. This is due to two opposite processes: on the one hand, the probability of the generation of TiC particles increases, on the other hand, their coagulation occurs.

Feasibility of producing ultra-high performance concrete with high elastic modulus by steel chips: An experimental study

Elastic modulus is one of the key parameters to weigh the stiffness of concrete members and structural design in civil engineering. Despite its excellent performance in durability and mechanical properties, ultra-high performance concrete (UHPC) is featured with relatively low elastic modulus, which prevents UHPC from being applied in a much larger scope. This study was conducted to explore the feasibility of preparing UHPC with high elastic modulus (HMUHPC) by using steel chips. The modified Andreasen and Andersen (MAA) particle packing model was used to design the initial mixture of HMUHPC. Based on this, some steps were followed to investigate the impacts of varying contents of steel chips on HMUHPC with regard to its mechanical properties, workability, and apparent density. In addition, attention was also paid to how steel chips affected the microstructure of HMUHPC and the ultrasonic pulse velocity (UPV) propagated in HMUHPC. It was found that: 1) Due to the addition of steel chips, there was an increase from 9.65% to 21.73%, 6.38% to 15.85%, 1.28% to 10.49%, and 3.11% to 16.44%, respectively, in the elastic modulus, compressive strength, flexural strength, and apparent density of HMUHPC; 2) The addition of steel chips could reduce the porosity of HMUHPC and optimize its pore size distribution; 3) Considering the effects of steel chips on HMUHPC regarding its microstructure, mechanical properties, and workability, the optimal content of steel chips in HMUHPC was 50 wt%.

Solid–Liquid Equilibrium in Co-Amorphous Systems: Experiment and Prediction

In this work, the solid-liquid equilibrium (SLE) of four binary systems combining two active pharmaceutical ingredients (APIs) capable of forming co-amorphous systems (CAMs) was investigated. The binary systems studied were naproxen-indomethacin, naproxen-ibuprofen, naproxen-probucol, and indomethacin-paracetamol. The SLE was experimentally determined by differential scanning calorimetry. The thermograms obtained revealed that all binary mixtures investigated form eutectic systems. Melting of the initial binary crystalline mixtures and subsequent quenching lead to the formation of CAM for all binary systems and most of the compositions studied. The experimentally obtained liquidus and eutectic temperatures were compared to theoretical predictions using the perturbed-chain statistical associating fluid theory (PC-SAFT) equation of state and conductor-like screening model for real solvents (COSMO-RS), as implemented in the Amsterdam Modeling Suite (COSMO-RS-AMS). On the basis of the obtained results, the ability of these models to predict the phase diagrams for the investigated API-API binary systems was evaluated. Furthermore, the glass transition temperature (Tg) of naproxen (NAP), a compound with a high tendency to recrystallize, whose literature values are considerably scattered, was newly determined by measuring and modeling the Tg values of binary mixtures in which amorphous NAP was stabilized. Based on this analysis, erroneous literature values were identified.

Thermal runaway evaluation on batch polyvinyl acetate emulsion polymerization from calorimetric measurement.

Emulsion polymerization is the most applied method in the vinyl acetate monomer (VAM)-polyvinyl acetate (PVAc) process. However, the flammable property and unexpected bulk polymerization for the reactant and product may occur in the batch reactor or storage tank. VAM is reactive enough to decompose readily into free radicals and then, initiate the polymerization, which may contribute to heat accumulation due to the monomer, initiator, and solvent mixtures. This study attempts to analyze the exothermic reaction and compare the thermal runaway potential for various VAM solutions during PVAc polymerizations. Summarily, 50%, 70%, and 100% of VAM solutions reacting with 2,2'-azobis(2-methylpropionitrile) readily increase the self-heating rate with their concentration from adiabatic calorimetric tests. Furthermore, kinetic parameters of 50, 70, and 100 mass% VAM solutions were evaluated to elucidate the self-heating model associated with thermal analysis and to determine heat production mechanisms that are practical to proactive safety protocol for the PVAc emulsion process.

Adaptive simulations of flame acceleration and detonation transition in subsonic and supersonic mixtures

Two-dimensional simulations were carried out to investigate the flame acceleration and deflagration-to-detonation transition (DDT) in a combustion chamber filled with a subsonic or supersonic mixture by employing Navier-Stokes equations together with a detailed chemistry reaction mechanism of 11 species and 27 steps under adaptive mesh refinement. The effects of the initial mixture Mach number and mesh resolution on the flame acceleration and DDT were studied in detail, and the entire processes of the flame acceleration, DDT and detonation propagation were revealed. Two DDT mechanisms are obtained in a chamber having the same low blockage ratio but with different initial velocities of the mixture. Regime I: multiple shock wave collisions, shock focusing and shock reflection result in a rapid energy deposition in a small region; a direct detonation subsequently occurs in the boundary wall for the subsonic mixture. Regime II: the classic hot-spot mechanism due to the reactive gradient mechanism is responsible for the detonation transition in the supersonic mixture when the intense leading shock wave impacts and reflects on the solid surface. By increasing the initial mixture Mach number, the run-up time and distance to DDT are dramatically reduced. The flame front structure and propagation in the supersonic flow demonstrate that the detonation cell size rapidly increases when propagating into the smooth region due to detonation attenuation and resulting pressure decrease. Additionally, a much higher combustion temperature occurs in the upper and lower walls because of the Mach stem. In comparison, the results show that the detonation overdrive degree and pressure gain ratio in the subsonic mixture are higher than in the supersonic mixture. Moreover, flame propagation upstream also suggests that increased pressure and temperature occur in the inlet isolation section, even forming a localized explosion point.

Towards understanding the effect of fibrinogen interactions on fibrin gel structure.

Fibrin gelation involves the enzymatic conversion of the plasma protein fibrinogen to fibrin monomers which then polymerize to form the gel that is a major structural component of a blood clot. Because fibrinogen provides the material from which fibrin is made, it is generally regarded as promoting the gelation process. However, fibrinogen can bind to a site on a fibrin oligomer, preventing another fibrin oligomer from binding there, thus slowing the polymerization process. "Soluble fibrin oligomers," which are mixtures of fibrin and fibrinogen, are found in the blood plasma and serve as biomarkers for various clotting disorders, so understanding the interplay between fibrin and fibrinogen during fibrin polymerization may have medical importance. We present a kinetic gelation model of fibrin polymerization which accounts for the dual and antagonistic roles of fibrinogen. It builds on our earlier model of fibrin polymerization that proposed a novel mechanism for branch formation, which is a necessary component of gelation. This previous model captured salient experimental observations regarding the determinants of the structure of the gel, but did not include fibrinogen binding. Here, we add to that model reactions between fibrinogen and fibrin, so oligomers are now mixtures of fibrin and fibrinogen, and characterizing their dynamics leads to equationsof substantially greater complexity than previously. Using a moment generating function approach, we derive a closed system of moment equationsand we track their dynamics until the finite time blow-up of specific second moments indicates that a gel has formed. In simulations begun with an initial mixture of fibrin and fibrinogen monomers, a sufficiently high relative concentration of fibrinogen prevents gelation; the critical concentration increases with the branch formation rate. In simulations begun with only fibrinogen monomers that are converted to fibrin at a specified rate, the rates of conversion, fibrinogen binding to oligomers, and branch formation together determine whether a gel forms, how long it takes to form, and the structural properties of the gel that results.

Study on MoS2/Fe‐MIL‐88NH2 Transition metal dichalcogenide/Metal‐organic framework as a novel composite for highly adsorption of methylene blue dye from aqueous solutions

The present study proposes a unique MoS2/Fe‐MIL‐88NH2 composite as an adsorbent for methylene blue (MB) from aqueous solutions for the first time. Different physicochemical techniques are utilized to characterize (metal–organic framework [MOF]/transition metal dichalcogenide [TMD]), including elemental analysis, Fourier transform infrared (FT‐IR), field emission scanning electron microscopy (FE‐SEM), zeta potential (ζ) measurement, and Brunauer–Emmett–Teller (BET) theory. The effects of different process factors on MB dye adsorption by composite are examined, including initial dye concentration, adsorbent loading, solution pH, temperature, and dye mixture. Various process parameters encompassing the initial dye concentration, adsorbent loading, solution pH, temperature, and mixture of dyes are investigated, and the equilibrium adsorption capacity towards MB is found up to 370 mg g−1 (when pH = 4.0, contact time is 90 min, and the adsorbent dose is 0.0068 mmol g−1). Experimental results reveal that the adsorption process is highly dependent on adsorbent dosage, initial MB concentration, and aqueous solution temperature. Equilibrium data are fitted onto Langmuir, Freundlich, Temkin, and Dubinin–Radushkevich models expressing the MB adsorption phenomena. Moreover, the isotherm data fit Freundlich mathematical models with maximum dye adsorption of 370 mg g−1. Sorption kinetics follows a pseudo‐second‐order model.