Qm Value Research Articles

Removal of As(V) and Cr(VI) using quinoxaline chitosan schiff base: synthesis, characterization and adsorption mechanism

Elevated Arsenic and Chromium levels in surface and ground waters are a significant health concern in several parts of the world. Chitosan quinoxaline Schiff base (CsQ) and cross-linked chitosan quinoxaline Schiff base (CsQG) were prepared to adsorb both Arsenate [As(V)] and Chromium [Cr(VI)] ions. The thermo-gravimetric analysis (TGA), X-ray diffraction analysis (XRD), and Fourier-transform infrared spectroscopy (FTIR) were used to investigate the prepared Schiff bases (CsQ) and (CsQG). The UV–VIS spectra showed a shift in the wavelength area of the modified polymer, indicating the reaction occurrence, besides the variation of the shape and intensity of the peaks. The XRD patterns showed the incensement of the amorphous characteristic. On the other hand, the thermal stability of the modified polymers is better according to TGA studies; also, the morphology of the modified chitosan was investigated before and after crosslinking (CsQ and CsQG) using a scanning electron microscope (SEM) where the surface was fall of wrinkles and pores, which then were decreased after cross-linking. Contact time, temperature, pH, and initial metal ion concentration were all studied as factors influencing metal ion uptake behavior. The Langmuir, Temkin, Dubinin–Radushkevich, and Freundlich isotherm models were used to describe the equilibrium data using metal concentrations of 10–1000 mg/L at pH = 7 and 1 g of adsorbent. The pseudo-first-order and pseudo-second-order kinetic parameters were evaluated. The experimental data revealed that the adsorption kinetics follow the mechanism of the pseudo-second-order equation with R2 values (0.9969, 0.9061) in case of using CsQ and R2 values (0.9989, 0.9999) in case of using CsQG, demonstrating chemical sorption is the rate-limiting step of the adsorption mechanism. Comparing the adsorption efficiency of the synthesized Schiff base and the cross-linked one, it was found that CsQ is a better adsorbent than CsQG in both cases of As(V) and Cr(VI) removal. This means that cross-linking doesn’t enhance the efficiency as expected, but on the contrary, in some cases, it decreases the removal. In addition, the newly modified chitosan polymers work better in As(V) removal than Cr(VI); the removal is 22.33% for Cr(VI) and 98.36% for As(V) using CsQ polymer, whereas using CsQG, the values are 6.20% and 91.75% respectively. On the other hand, the maximum adsorption capacity (Qm) for As(V) and Cr(VI) are 8.811 and 3.003 mg/g, respectively, using CsQ, while in the case of using CsQG, the Qm value reaches 31.95 mg/g for As(V), and 103.09 mg/g for Cr(VI).

The high adsorption performance of banana (Musa ABB Cv. Kluai ‘Namwa’) beaded materials modified with zinc and magnesium oxides for cadmium removal

Wastewater contaminated with cadmium is a concern because of its toxicity, persistence, and bioaccumulation to the environment, ecosystem, and human health, so it is required to remove cadmium(II) ions before releasing them to receiving water. Banana powder beads (BPB), banana powder doped ZnO beads (BPZB), banana powder doped MgO beads (BPMB), and banana powder doped ZnO + MgO beads (BPZMB) were synthesized as the novel cadmium adsorbents, and their characterizations, cadmium adsorption performances, cadmium adsorption patterns and mechanisms, thermodynamic study, and reusability were investigated. BPMB had the highest specific surface area of 16.60 m2/g and the smallest pore size of 1.69 nm than other materials. BPB was an amorphous structure, whereas BPZB, BPMB, and BPZMB were crystalline structures presenting their specific metal oxide peaks of ZnO or MgO. They were coarse surfaces and had a spherical shape consisting of C, O, Ca, Cl, and Na. Their main functional groups were O–H, C–H, C=O, C–O, and N–H. The points of zero charge of BPB, BPZB, BPMB, and BPZMB were 5.37, 6.75, 9.87, and 9.43. The cadmium removal efficiencies of BPB, BPZB, BPMB, and BPZMB were 89.18%, 96.62%, 99.59%, and 97.85%, and their qm values were 90.09, 232.56, 454.55, and 303.03 mg/g, respectively. Thus, the metal oxide helped to improve material efficiency, especially MgO. The Freundlich and pseudo-second-order kinetic models were good fit models for describing their adsorption patterns and mechanisms. The increasing temperature affected to decrease their cadmium adsorptions. They could be reused in more than 3 cycles of more than 73% of cadmium adsorption. The electrostatic interaction played an important role in describing their cadmium adsorptions. Therefore, BPBM was a good cadmium adsorbent for application in industrial wastewater treatment since it had a higher performance of cadmium adsorption than other materials.

Heavy metal adsorption on yellow loam clay modified by biomass- and biochar-decomposed liquids from Ficus microcarpa

In studing the heavy metal adsorption effect of decomposed liquid (Dl) on yellow loam clay (C), biomass-Dl (BmDl) and biochar-Dl (BcDl) from Ficus microcarpa leaves were used to modify C. The different Dl-modified Cs (Dl-Cs) were characterized by scanning electron microscopy and Fourier transform infrared spectroscopy. A batch method was used to study the adsorption kinetics and thermodynamics of Pb(II) and Cd(II), as well as the effects of decomposition time, modification ratio, pH, temperature, and ionic strength on the adsorption process. Results of microscopic morphology indicated that Dl was modified on the C surface, and it changed the surface properties. The adsorption isotherms of Pb(II) and Cd(II) by different Dl-Cs conformed to the Langmuir and Freundlich model, with the maximum adsorption capacity (qm) maintained at 65.64–163.89mmol/kg (BmDl-Cs) and 77.68–235.63mmol/kg (BcDl-Cs). Under the same conditions, the peak value of qm was reached at decomposition time of 14 days and 50% of Dl modification. pH = 6, ionic strength of 0.1mol/L, and 30 ℃ were the optimum conditions for the adsorption of Pb(II) and Cd(II) by different Dl-Cs. Pb(II) and Cd(II) adsorption was a spontaneous, endothermic, and entropy-increasing process, and pseudo-first-order kinetic equation was suitable to characterize adsorption.

Sodium alginate- and chitosan-based hydrogels with different network charges for selective removal of cationic and anionic dyes from water

ABSTRACT The grafting of chitosan (CH) and sodium alginate (SA) biopolymers with glycidyl methacrylate (GMA) and acrylamide (AAm) monomers, combined with graphene oxide (GO), led to the formation of bio-based hydrogels. These hydrogels, named CH -GO -hydrogel (GO/CH-g-poly (AAm-co-GMA)), CH -GO -hydrogel (CH-g-poly (AAm-co-GMA)), SA -GO -hydrogel (GO/SA-g-poly(AAm-co-GMA)), and SA -hydrogel (SA-g-poly(AAm-co-GMA)), were tested as selective dye adsorbents. While the chitosan-based hydrogels exhibited positive zeta potential values ranging from +27.5 to +0.1 mV, alginate-based samples had negative values between −10.4 to −41.7 mV in pH conditions from 3.0 to 9.0. Adding GO nano-fillers reduced the swelling capacity of both hydrogels, with water absorption (WA) values for SA -GO -hydrogel and SA -hydrogel recorded at 10.1 and 22.2 g/g, respectively. The ability of these materials to adsorb dyes, specifically crystal violet (cationic) and Congo red (anionic), was confirmed. Factors such as adsorbent dosage, initial pH, dye concentration, shaking time, and temperature were analyzed to determine dye adsorption capacity. Interestingly, the pristine hydrogels, free of GO, performed better than their nanocomposite counterparts. Adsorption capacities (qm) for crystal violet and Congo red with SA -hydrogel, SA -GO -hydrogel, CH -hydrogel, and CH -GO -hydrogel was 909.1, 714.3, 454.5, and 400.0 mg/g, respectively.

Adsorption behavior and mechanism of different types of (aged) microplastics for napropamide in soils

The role of microplastics (MPs) as pollutant carriers and their influence on the fate of organic pollutants has received considerable attention. However, the impacts of MPs on the adsorption of amide herbicides in soil, have not been investigated. In this study, non-biodegradable (polyethylene, PEM) and biodegradable (polybutylene adipate terephthalate, PBATM) MPs were aged by exposure to one month of ultraviolet irradiation. The impacts of MPs on the adsorption of napropamide (Nap) in two agricultural soils (black soil [BS] and fluvo-aquic soil [CS]) were investigated through batch experiments. The findings suggested that the adsorption of Nap onto PEM was mainly governed by physical processes, while, chemical mechanisms, should not be overlooked on PBATM. With the addition of 0.2% MPs, the maximum adsorption capacity (Qm) and adsorption distribution coefficient (KF) of soil containing PEM (soil-PEM) were higher than that of soil-PBATM, however, the Qm and KF values of soil-PBATM for Nap were higher when the addition of MPs was 2%. After UV aging, the increased specific surface area of MPs led to an increased adhesion of soil particles. These were attributed to the different surface properties and concentrations of different (aged) MPs, resulting in differences in the inhibition effect by soil particles. The adhesion of soil particles was confirmed by X-ray photoelectron spectroscopy. Additionally, regardless of the addition of MPs, the Qm values of BS for Nap were higher than those for CS. In summary, MPs can alter the adsorption of Nap in soil, influencing both its mobility within the soil ecosystem and the environmental risk.

Improvement on Qm in high-power piezoelectric ceramics through [111]c texture engineering

Improving mechanical quality factor Qm is of great significance for high-power applications. Here, a new strategy of the [111]c texture engineering was proposed to enhance the performances of high-power piezoelectric ceramics. The 5 vol% BaTiO3 (BT) templates with the [111]c preferred orientation were introduced into matrix powders of 0.03 Pb(Mn1/3Nb2/3)O3–0.33Pb(Ni1/3Nb2/3)O3–0.28 PbZrO3–0.36PbTiO3 (28PZ(R)) to form the [111]c textured ceramics (28PZ(T)), possessing a texture degree of 74 %. The multiple of uniform density in EBSD increased from 0.63 in randomly oriented 28 PZ(R) to 6.63 in 28PZ(T). The good lattice matching between BT templates and textured grains was observed using high-resolution transmission electron microscopy, confirming the microscopic origin of the [111]c texture. The maximum phase angle θmax of 88.2° was quite near 90° in 28PZ(T), ensuring the optimal Qm value of 1275 and the great figure of merit of 255,000 pC/N. The increased Qm in [111]c texture ceramics was confirmed due to the reduced intrinsic polarization directions rather than the pinning effect of the internal bias field. Larger grain sizes with larger domains restrained the movement of domain walls in 28 PZ(T), which was also favorable to higher Qm. This work may provide a new promising route for further high-power applications.

Effects of carbonization on the structure and sorption properties of coffee grounds for Pb(II) and Ni(II) in various metal systems

Two biochars (i.e., Mu@CG and Tu@CG) derived from waste coffee grounds (CG) were prepared and muffle furnace (Mu) and tube furnace (Tu) were utilized to inspect the impact of carbonization process. It indicated that the specific surface area of Mu@CG could reach 124.26 m2/g, which was 37 times higher than that of Tu@CG (3.288 m2/g). Sorption experiments revealed that the optimal conditions were 55 °C, pH= 4, time= 10 h, and concentration was 80 mg/L for both combustion furnaces. Specifically, Mu@CG exhibited larger pore size (3.42 nm) than Tu@CG (0.015 nm), suggesting that Mu can increase the pore size of CG. The sorption of Pb(II) and Ni(II) on Mu@CG and Tu@CG followed pseudo-1st-order kinetic model. The Langmuir qm value of Mu@CG for Pb(II) was 67.037 mg/g. While, the cycle times of Mu@CG for Pb(II) and Ni(II) can be arrived at 5 times and HCl is an ideal de-sorbent for the regeneration of Mu@CG for Pb(II) and Ni(II). Further, the negative ∆G and positive ∆H data confirmed that Pb(II) and Ni(II) sorption on Mu@CG and Tu@CG were spontaneous and endothermic processes. Based on these findings, it can be concluded that for CG pyrolysis, muffle furnace will be one of the most favorable manners.

Quaternary piezoelectric ceramics with ultra-high mechanical quality factor

The development of piezoelectric ceramics with large piezoelectric coefficient (d33), high Curie temperature (TC) and high mechanical quality factor (Qm) is still a key challenge for practical application for high-power device. Herein, a novel quaternary piezoelectric ceramics of (0.125-x) Pb0.98Sr0.02(Mg1/3Nb2/3)O3–0.445PbTiO3–0.43PbZrO3-xPb(Mn1/3Nb2/3)O3 (abbreviated as xPMnN-PSMN-PZT) were prepared by the solid-state sintering method. The hard dopant PMnN induced the morphotropic phase boundary (MPB) of PSMN-PZT into a tetragonal-rich region. In addition, the XPS and EPR analysis proved the existence of a large amount of oxygen vacancies (Vo••) in PMnN-PSMN-PZT ceramic system. The composition near tetragonal-rich MPB region and the appearance of defect dipoles formed a strong coupling effect on the domain wall motion and leaded to an ultra Qm value. The optimum piezoelectric properties were achieved at x = 9 mol% with d33 = 260 pC/N, Qm = 3880, tanδ = 0.009 and TC = 332 °C. A significant internal bias field (Ebias) of 8.83 kV/cm was also observed in 0.09PMnN-PSMN-PZT ceramics. The origin of this excellent piezoelectric properties was explained by the phase structure, piezoelectric and dielectric analysis. This work demonstrated a rational strategy to obtain ultra Qm value for high-power piezoceramics.

One stone, two birds: An eco-friendly aerogel based on waste pomelo peel cellulose for the efficient adsorption of dyes and heavy metal ions

To achieve the objective of “waste control by waste”, in this study, a green aerogel adsorbent comprised of pomelo-peel cellulose and sodium alginate (PCC/SA) was prepared through dual-network crosslinking. The resulting 3D hierarchical porous structured PCC/SA aerogel exhibited good structural stability, and kept the morphological integrity during 10 days in a wide pH range (2–10), suggesting its potential for recycling in diverse complex environments. Besides, the superior adsorption capacities for methylene blue (MB) and Cu(II) were observed, with the qm values and adsorption equilibrium times were recorded to be 1299.59 mg/g (300 min) and 287.55 mg/g (120 min), correspondingly. Furthermore, the favorable reusability of the PCC/SA aerogel was also demonstrated, with the removal efficiency for MB remaining almost unchanged (about 94 %) after 10 adsorption-desorption cycles, while there was a slight reduction for Cu(II) from 85.28 % to 72.47 %. XPS and FTIR analysis revealed that electrostatic attraction, hydrogen bonding, cation exchange and coordination were the major adsorption mechanisms. Importantly, the PCC/SA aerogel can be naturally degraded in soil within 10 weeks. Therefore, the as-prepared aerogel bead derived from pomelo peel shows great promise as an adsorbent for wastewater treatment containing dye and heavy metal ions.

Nonlinearly charged black holes: Shadow and thin-accretion disk

In this paper, we explore the effect of the parameters of non-linear electrodynamics (NLED) and magnetic charges on various aspects of black holes (BH) arising in the particular NLED theory. More precisely, we look into the behavior of photons around the BH and produce shadow by considering a thin accretion disk model. We initially examine the overall behavior of the photon sphere and the corresponding shadow silhouette under the effects of these parameters. Using the EHT data for Sgr. A* and M87*, we provide constraints on the magnetic charge qm. Our results indicate that M87* gives better constraints, and as the value of the NLED coupling parameter β is increased, the constrained range for qm widens. At lower values of qm, we find that the shadow radius is close to the observed value. Then, we study different other aspects, such as the energy emitted by the accretion disk, the temperature of the disk around the BH, and the nature of light it gives off. We also look at how the black hole shadow appears in different situations. Finally, we investigate how the magnetic charge affects all the above mentioned aspects when we take into account NLED along with gravity. This study helps us understand the complex relationship between magnetic charge and its effect on various aspects related to a BH.

Modification of domain construction in PNN-PIN-PT piezoelectric ceramics for high electromechanical performance using defect engineering

Good piezoelectric properties and low mechanical losses are prerequisites for the application of high-power devices. In this study, an appropriate amount of Mn ions was introduced into a piezoelectric 0.46Pb(Ni1/3Nb2/3)O3-0.23Pb(In1/2Nb1/2)O3-0.31PbTiO3 ceramic to enhance its electromechanical properties. The results revealed that the mechanical quality factor(Qm) value of the ceramic was improved while maintaining high piezoelectric properties, and the dielectric loss was reduced. When Mn doping is 1.0 mol%, the d33 component decreased by only ∼21%, while Qm increased by ∼13 times (d33 = 750 pC/N, Qm = 385, tanδ = 0.66%). The measurement of the internal bias field (Ei) in the P-E loops of aged and nonaged samples showed that aging promoted the directional alignment of defect dipoles and improved their Qm. According to the PFM data, significant increase in Qm was mainly due to the "bulk effect" caused by low domain wall density. In turn, widening and lengthening of domains promoted the accumulation of most defective dipoles in the ceramic body, which greatly amplified the hardening effect. This work provides a good example of enhancing Qm in ceramic systems with high d33 values through the construction of low domain wall densities.

Synthesis of Na-Alginate templated Montmorillonite-Silica Composite as adsorbent for removal of Rhodamine B

In this study, mesoporous Montmorillonite-Silica composites prepared by using different amount Alginate as sacrificial template, for removal of Rhodamine B is investigated. By alternating Alginate amount it is aimed to switch the porosity of adsorbents thus the adsorption capacities of adsorbents. Synthesized adsorbents had been characterized by using Scanning Electron Microscopy, X-ray diffraction, Fourier transform infrared spectroscopy and N2-Ads/Des techniques. It is observed that beside the decrease in the micropore volume, the total pore volume of the adsorbents increased with the increasing of used Alginate amount. The total pore volumes of adsorbents synthesized with different Clay/Alginate ratio (10, 5, 1) were found as 0.116, 0.172, and 0.178 cm3/g, respectively. Batch adsorption studies showed that the maximum removal efficiencies were obtained at acidic conditions and the adsorbents had better fit with Freundlich isotherm. Qm values obtained from Langmuir isotherm were found as 24.47, 31.97 and 28.48 mg/g for synthesized adsorbents. Also, adsorption kinetic studies showed that for all adsorbents, experimental data had good fit to the pseudo-second order kinetics model. The model parameters were found as 5.9,6.3 and 6.5 (10–3 g/ (mg min). Thermodynamic parameters were also investigated in the study. Negative ∆Go values pointed out that the adsorption of RhB onto synthesized adsorbents was favorable process. Positive values of ∆Ho and ΔS indicated that the adsorption of RhB on adsorbents were endothermic and rising of randomness during the adsorption of RhB on the surface of the adsorbent. Adsorbents could be recovered at least five times without significant decrease in adsorption capacity.

Mechanism and application of lead-free KNN-based ceramics with superior piezoelectricity

Piezoelectric ultrasonic energy harvesters (PUEHs) have recently attracted increasing attention. For minimizing the energy losses during energy transfer, it is crucial for core piezoelectric materials to maintain high piezoelectric coefficient (d33), mechanical quality factor (Qm), and piezoelectric voltage coefficient (g33). Herein, a simple way of hardening strategy improves the piezoelectric properties of KNN-based ceramics, combined with optimizing grain growth. The enhanced d33 (∼340 pC/N), high Qm (∼211) and TC (∼305 °C) are obtained simultaneously in this system, accompanied by superior d33×g33=8770×10−15 m2/N. Through variable temperature resonance test, the polarization rotation diversity caused by phase structure difference is found to closely related to the temperature stability of Qm value. A prototype of PUEH device was further designed and fabricated, with adjustable ultrasound-induced output voltage up to 8.2 V. Our work exhibits an effective way to improve performance of PUEHs by optimizing piezoelectric materials, which is helpful for further developing PUEHs.

Highly efficient sorbent utilizing regenerated cellulose as an eco-friendly template for humic acid removal and oil–water separation processes

In this study, a novel and environmentally friendly sorbent was developed utilizing regenerated cellulose (RC) as a renewable resource. The preparation process of the regenerated cellulose hydrogel, following a bottom-up strategy, occurs in an aqueous system and offers the added benefits of temperature-induced gelation and solvent recyclability. The RC/PEI aerogel was prepared through a polyethyleneimine (PEI) modification and di-epoxide crosslinking process, which improves the gel's elastic recovery for the squeezing process and concurrently provides excellent ability to remove humic acid (HA) contaminants. As a result of the HA removal experiment using the RC/PEI aerogel in an aqueous environment, the gel showed an experimental HA adsorption capacity of 124.9 mg/g and qm value of 196.7 mg/g. Furthermore, the prepared RC hydrogel template was successfully transformed into a highly effective oil–water separation sorbent through a hydrophobic alkylated graphene oxide (AGO) coating process. Oil-water separation was carried out using AGO-RC/PEI gel, and it was possible to successfully adsorb the oil and then recover it through the squeezing process. In addition, long-term usability has been validated by demonstrating an oil adsorption capacity of over 84 %, even after ten consecutive reuses.

Synthesis and characterization of surface-modified magnetic mesoporous silicate materials for phosphate adsorption.

The magnetic mesoporous silica material, Mag-MCM-41, was synthesized by coating magnetite (Fe3O4) nanoparticles with a mesoporous material called MCM-41. Mag-MCM-41 and modified nanomaterials Mag-MCM-41-NN and Mag-MCM-41-NN-Fe+3 which were modified with aminopropyl functional groups. In water and wastewater, phosphate anions are considered significant contaminants due to their detrimental impact on the environment. They promote the growth of algae, leading to eutrophication. The purpose of this study is to investigate the removal of phosphate anions from aqueous solutions using modified magnetic silica particles. The Mag-MCM-41 material exhibits hexagonal properties and belongs to the class of "mesoporous" materials. It has a surface area of 923 m2.g-1, which was determined through N2 adsorption-desorption isotherms, FTIR, TEM, BET, and SAXS analysis. Kinetic and adsorption isotherm studies were conducted using Mag-MCM-41, Mag-MCM-41-NN, and Mag-MCM-41-NN-Fe+3 adsorbents to examine the behavior of phosphate anions. The kinetic and adsorption isotherm studies of phosphate anions revealed that the adsorption process on Mag-MCM-41, Mag-MCM-41-NN, and Mag-MCM-41-NN-Fe+3 adsorbents followed the chemical adsorption mechanism. Phosphate adsorption on all adsorbents occurred in a monolayer, and the MCM-41-NN-Fe+3 adsorbent exhibited the highest maximum adsorption capacity (qm) value of 112.87 mg.g-1 compared to the other adsorbents.

Comparative Investigation of Phosphate Adsorption Efficiencies of MOF-76 (Ce) and Metal Oxides Derived from MOF-76 (Ce).

Phosphate pollution is a very challenging problem for the water environment. Phosphate mixed with water in various ways causes eutrophication. To sustain life in aquatic systems, phosphate ions must be cleaned. Therefore, it is very important to remove phosphate in wastewater. Here, an adsorption method has been tried for the removal of phosphate. MOF-76 (Ce), a cerium-based metal-organic framework, was synthesized by a hydrothermal method. Since metal oxides are known to be successful in phosphate adsorption, CeO2 nanoparticles were also obtained by pyrolysis of this MOF structure. The phosphate adsorption efficiencies of both adsorbents were compared. The characterization methods (SEM, FTIR, XRD, and TGA) were applied to adsorbents. The kinetic, isotherm, and thermodynamics studies were applied to experimental results. At 298 K, the adsorption capacity of MOF-76 (Ce) is higher than that of CeO2, according to Langmuir isotherm qm values. The qm values are 72.97 and 55.71 mg/g, respectively. Both adsorbents follow the pseudo second-order kinetic model. It has been found that MOF-76 (Ce) has a pH-selective property in phosphate adsorption. No change was observed in the phosphate adsorption capacity of CeO2 with pH. In terms of thermodynamics, the endothermic reaction is valid for both adsorbents.

Methylene Blue Removal by Copper Oxide Nanoparticles Obtained from Green Synthesis of Melia azedarach: Kinetic and Isotherm Studies

In this study, Melia azedarach fruit extract was used as a reducing agent and copper chloride dihydrate (CuCl2·2H2O) was used as a precursor in the synthesis of copper oxide nanoparticles (CuO NPs). The UV–visible spectrum showed a characteristic absorption peak of CuO NPs at 350 nm. The surface properties of the adsorbent were analyzed through various techniques, indicating the successful formation of CuO NPs. The impacts of several factors, including initial pH (4 to 8), a dose of CuO NPs adsorbent (0.01–0.05 g), dye initial concentration (10–50 mg·L−1), and contact times ranging from 5 to 120 min, were examined in batch adsorption studies. Based on the experimental results, the Langmuir isotherm is well-fitted, indicating MB dye monolayer capping on the CuO NPs surface with 26.738 mg·g−1 as a maximum adsorption capacity Qm value. For the pseudo-second-order kinetic model, the experimental and calculated adsorption capacity values (qe) exhibited good agreement.

Efficient reactive adsorption of hexamethyldisiloxane on MCM-41 supported sulfuric acid

Volatile methyl siloxanes (VMSs), which are converted to silica sediments during biogas burning, are regarded as the most problematic VMSs in existing biogas cleaning systems. However, the majority of methods for VMS removal, including cryogenic condensation, physical absorption, chemical absorption and porous material adsorption have been constrained by these methods' intrinsic drawbacks. Here, we present an alternate method for removing VMS from gas streams that are based on the materials supported by H2SO4. Simple incipient wetness impregnation was used to create MCM-41-supported H2SO4 (SSA/MCM) materials, which showed high reactive adsorption property for hexamethyldisiloxane (L2) elimination in the temperature range of 80–160 °C with the peak reactivity at 100 °C. With maximum QB and Qm values of 191.3 and 365.6 mg g−1, respectively, dynamic adsorption findings showed the significance of altering the intake concentration, gas flow rate, adsorbent mass, relative humidity, as well as H2SO4 loading in determining the L2 removal efficacy. Furthermore, it was established that the L2 reactive adsorption was caused by the polymerization of L2 by supported H2SO4, which produced the creation of polysiloxane. The findings offer an important foundation for creating a cutting-edge biogas cleaning method.

Arsenic removal adsorbent using limonite-polyethersulfone composite fiber via continuous flow column process.

This research introduces an enhanced limonite-based composite fiber adsorbent for arsenic (As) removal. The modification involves creating polyethersulfone (PES)-limonite composite fibers loaded with 60 wt% limonite powders, designed to be applicable in water flow environments. The fibers were prepared using a wet-spinning process based on phase inversion, with varying concentrations (10, 20, and 30 wt%) of PES in NMP solution. The composite fiber with 10wt% NMP exhibited a porous structure and demonstrated efficient absorption of both As(III) and As(V). Adsorption followed the Langmuir model, with qm values of 1.5mg/g for As(III) and 3.2mg/g for As(V) at pH6. In column experiments, As removal rates increased with contact time, attributed to decreased flow rates (1mL/min). Moreover, increasing fiber column height led to enhanced removal rates, as indicated by the Adams-Bohart model. The mechanism for As(V) removal involved the formation of an inner-sphere complex through ion exchange between α-FeOOH and HAsO4 - and H2 AsO4 2- in an aqueous solution at pH6.8. PRACTITIONER POINTS: Changing the polyethersulfone ratio in the composite leads to variations in the appearance of limonite within each composite fiber. Limonite composite fibers effectively remove As(III) and As(V) at neutral pH. The adsorption behavior follows Langmuir kinetic model, the qm of 1.5mg/g for As(III) and 3.2mg/g for As(V). Longer columns and contact times enhance arsenic (As) removal in practical water treatment systems. Adam-Bohart model aids in predicting breakthrough and saturation time in As adsorption column design.

Spatiotemporal Variations of the Frequency-Magnitude Distribution in the 2019 Mw 7.1 Ridgecrest, California, Earthquake Sequence.

Significant seismic activity has been witnessed in the area of Ridgecrest (Southern California) over the past 40 years, with the largest being the Mw 5.8 event on 20 September 1995. In July 2019, a strong earthquake of Mw 7.1, preceded by a Mw 6.4 foreshock, impacted Ridgecrest. The mainshock triggered thousands of aftershocks that were thoroughly documented along the activated faults. In this study, we analyzed the spatiotemporal variations of the frequency-magnitude distribution in the area of Ridgecrest using the fragment-asperity model derived within the framework of non-extensive statistical physics (NESP), which is well-suited for investigating complex dynamic systems with scale-invariant properties, multi-fractality, and long-range interactions. Analysis was performed for the entire duration, as well as within various time windows during 1981-2022, in order to estimate the qM parameter and to investigate how these variations are related to the dynamic evolution of seismic activity. In addition, we analyzed the spatiotemporal qM value distributions along the activated fault zone during 1981-2019 and during each month after the occurrence of the Mw 7.1 Ridgecrest earthquake. The results indicate a significant increase in the qM parameter when large-magnitude earthquakes occur, suggesting the system's transition in an out-of-equilibrium phase and its preparation for seismic energy release.