Endothermic Research Articles

Thermal radiation characteristic parameters of biomass mixed feedstock for concentrating solar gasification reaction

Solar energy and biomass are both important renewable energy, and the studies on them contribute to current goal of global carbon neutral. The solar gasification process directly employs solar radiation to drive the conversion from biomass to syngas via endothermic gasification reactions. This process relies on the biomass feedstock absorbing incident solar irradiation to sustain these reactions. The thermal radiation characteristics of biomass materials, such as spectral emissivity and absorptivity, determine its capacity for solar energy absorption versus losses from self-emission. Thus, these parameters are critical inputs for accurate thermal-balance modeling of the solar reactor. In this study, the reflectance of 9 biomass samples were experimentally measured in the main solar spectrum range of 200–2500 nm. Based on measurement results, the refractive index (n) and extinction coefficient (k) of each biomass materials are obtained via Kramers-Kronig relations. Besides, the dielectric function of the 9 biomass samples are also modeled using a 5-th Lorentz oscillator model and the model parameters are determined. The results indicate that the 5-th Lorentz oscillator model adequately characterizes the thermal radiation properties of diverse biomass feedstocks over the measured spectrum. This work contributes important spectral property data to enable accurate modeling and optimization of solar thermochemical conversion based on biomass gasification processes.

(Invited) Fundamentals of Plasmon-Induced Charge Transfer in Semiconducting Materials: Showcasing OER Catalysis

Using Localized Surface Plasmon Resonance Effect for Enhancing Electrochemical reactions has been reported earlier both in terms of direct electron injection/transfer (DET) in outer-sphere reductive processes as well as charge injection into semiconductors via plasmon-induced resonant electron transfer processes (PIRE). While the former (DET) is mainly influenced by the lifetimes of the ejected hot electrons and their rapid cooling at the interface. For inner sphere reductive processes via the LSPR phenomenon, direct charge injection into the LUMO states of the adsorbed species is required. In this regard, it is imperative to distinguish between the inter-band charge transfer of the adsorbed species because of exposure to photons.In contrast to these charge injections into semiconductors via plasmon-induced resonant electron transfer processes (PIRE), they must be more understood and complex. In this presentation, we will use the well-known endothermic anodic oxygen evolution reaction (OER) in alkaline pH to showcase the fundamental aspects of charge injection and its effect on the hole-driven OER mechanism. For this well-known OER catalyst, layered double hydroxides of Ni with Fe and Co dopants will be used. The electrochemical enhancement of OER will be explained based on detailed structural motifs of the semiconductors, its band structure, and the resonance effect of Au induced by the LSPR effect. Direct and indirect bandgaps will be discussed in the context of three possible mechanisms: (i) Charge carriers are directly injected into the semiconductor via LSPR. The semiconductor's conduction band is usually (-0.1 to 0.0 eV vs. NHE), and the valence band is between (2.00 and 3.5 eV), corresponding to electron energy between -2.00 to 3.5 eV vs. NHE. For LSPR nanoparticles, SPR energy is between 1.0 and 4.0 eV. Also, the Fermi energy of LSPR is usually 0.0 vs. NHE. Hence, LSPR only enables energetic electrons to be transferred from metals to semiconductors. It is the interface between LSPR and the semiconductor which is important. Charge injection is more prevalent when metal LSPR is of lower energy than the semiconductor—direct electron transfer (DET). (ii) Transfer does not involve direct electron injection but via (a) near-field electromagnetic and (b) resonant photon scattering mechanism. This has been shown to work by adding a thin dielectric material between the LSPR and the semiconductor. This would be most likely in the case of OER, where surface-localized plasmons will be the most important determinant instead of recombination events in the bulk of the semiconductor. This is most important for OER as it depends on the surface hole concentration. It should be noted that larger nanoparticles (>50 nm) have increased resonant photon scattering. Such a mechanism is more prevalent when we overlap metal LSPR and semiconductor bands, leading to plasmon-induced resonant electron transfer (PIRET). (iii) When metal LSPR is in direct contact with the semiconductor, all three phenomena could be active.

Investigation on thermochemical heat charging and discharging behavior of Ca(OH)2/CaO in a fixed bed reactor

Thermochemical heat storage (TCHS) technology plays a crucial role in the energy system, essential for maintaining the balance between energy supply and demand. The Ca(OH)2/CaO system holds significant promise for TCHS thanks to its high energy storage density, cost-effectiveness, and minimal heat loss. However, further research is required to elucidate the coupling mechanisms of the various physicochemical processes involved and to optimize the overall system performance. This paper focuses on assessing and elucidating the multi-physics coupled transport rules during both the charging and discharging stages in a fixed-bed reactor based on the developed numerical model. Results manifest the bed temperature rapidly increases to around 950 K, then slows down as the endothermic reaction predominates, completing dehydration in 1,900 s. During discharging, hydration conversion advances in a “U”-shaped pattern from the vapor inlet and side wall to the outlet, driven by the high vapor content near the inlet and the lower temperature near the wall. Furthermore, a thorough sensitivity analysis of the main parameters such as thermal conductivity and porosity is conducted to determine how different operating conditions affect the charging and discharging processes. Finally, a new reactor structure is proposed, in which a gas-guide duct is added at the central axis of the reactor to improve mass transport and uniformly distributed finned heating tube bundles to enhance heat transfer. These two functions can shorten the charging period by 9 % and 16 % respectively. The results can aid in predicting thermochemical conversion behaviors and multi-physic coupling transport processes, while also providing a foundational reference for the design of TCHS systems.

Removal of anionic dye from textile effluent using zirconium phosphate loaded polyaniline-graphene oxide composite: Lab to pilot scale evaluation

Efficient filtering of dyes is essential for the protection of ecosystem and human health due to the considerable water pollution caused by the effluents released from the sector. We present a simple, scalable UV radiation-assisted method for treating methyl orange dye-polluted water from the textile industry using zirconium phosphate-loaded polyaniline-graphene oxide (PGZrP) composite. The new material was synthesized by sonochemically incorporating a polyaniline-graphene oxide composite with hydrothermally synthesized zirconium phosphate. The efficacy of PGZrP in eliminating methyl orange was evaluated using experimental conditions, and the adsorption capacity was investigated as a function of pH, temperature, adsorbent dosage, and adsorption period. The system follows Langmuir adsorption isotherm with pseudo-second-order kinetics. Thermodynamics studies showed that enthalpy (H°) and entropy (S°) values are positive, indicating that the dye adsorption increases with increasing temperature and is an endothermic reaction. The maximum adsorption capacity was found to be 36.45379 mg/g for methyl orange. Using the COMSOL Multiphysics CFD Platform, an attempt was made to check the temperature and concentration profile of a PGZrP composite in a real industrial system. The predicted result shows that there is no significant temperature change in the material during the adsorption process and the concentration of dye is mainly located on the top region of the bed. The developed zirconium phosphate decorated polyaniline-graphene oxide composite can be successfully utilized for the effective removal of methyl orange from industrial wastewater in bulk quantity which is coming from the textile industry, and the composite can be reused for several cycles with good efficiency. In this work, we have designed a miniaturized proof of concept to remove methyl orange from water which showed good dye removal efficiency.

Efficient removal of polycyclic aromatic hydrocarbons from aqueous solutions using green cyclodextrin-maltodextrin nanosponge incorporated polyvinyl alcohol cryogel

Developing efficient adsorbents for removing polycyclic aromatic hydrocarbons (PAHs) from aqueous solutions is a significant and worthwhile approach. In this study, we showcase a method for fabricating β-cyclodextrin-maltodextrin nanosponges (βCD-MD) incorporated polyvinyl alcohol (PVA) cryogel for removing PAHs from aqueous solutions. The composite nanosponges enhanced the adsorption efficiency of PAHs such as Naphthalene, Acenaphthene, Fluorene, Phenanthrene, Anthracene, Fluoranthene, Pyrene, and Benzo[a]pyrene from water samples and the porous PVA cryogel helped to entrap and prevent the loss of the adsorbent. This efficacy was attributed to the strong affinities of PAHs toward βCD-MD nanosponges, facilitated by hydrophobic interactions between the analytes and the hydrophobic inner region present in both dextrins. The removal efficiency of the prepared βCD-MD/PVA composite cryogel was more than 95 % for all 8 PAHs (C0 = 5.0 mg/L) in less than 30 min, and the experimental data were well described by the Freundlich isotherm and the pseudo-second-order kinetic model. Additionally, the βCD-MD/PVA composite cryogel exhibited a maximum adsorption capacity ranging from 16.34 to 18.49 mg/g for eight PAHs. Moreover, the thermodynamic study revealed that the adsorption of PAHs was an endothermic and spontaneous process. The βCD-MD/PVA composite cryogel exhibited an abundance of polar functional groups along with numerous hydrophobic cavities and regions. It demonstrated high mechanical and thermal stability and maintained high removal efficiency even after seven adsorption–desorption cycles. Overall, it was concluded that βCD-MD/PVA composite cryogel can be utilized as a high-performance, eco-friendly, and sustainable alternative for PAH removal.

Kenaf Biochar as an Eco‐Friendly Adsorbent for Removal of Cu(II) and Pb(II): Optimal Temperature, Adsorption Models, and Efficiency Evaluation

ABSTRACTThis study examined the adsorption capacities of biochars derived from kenaf (KF‐BCs) for the removal of heavy metals such as Cu(II) and Pb(II). The thermal decomposition temperature (300–750°C) significantly influenced the morphology and composition of KF‐BCs, enhancing their surface area, pore structure, and alkalinity. Among them, kenaf pyrolyzed at 750°C (KF‐750) was the most effective in removing Cu(II) and Pb(II), as validated by kinetic, equilibrium, and isotherm model analyses. Adsorption kinetics revealed that equilibrium was attained after 24 h, with chemisorption governing the process rate. Equilibrium adsorption conformed to the Langmuir and Freundlich models for Cu(II) and Pb(II), respectively. KF‐750 exhibited midrange adsorption capacities for Cu(II) and Pb(II) (23.47 ± 0.3 mg/g and 50.07 ± 0.9 mg/g, respectively), compared with the literature. The thermodynamic assessment revealed an endothermic process with positive ∆H0, indicating that higher temperatures favor metal adsorption. At low pH, adsorption decreased due to electrostatic repulsion, particularly affecting Cu(II). More than 99.8% of Cu(II) and Pb(II) were removed with a 5.00 g/L KF‐750 dose. The cation effect order on KF‐750 was Ca2+ > Mg2+ > Na+ > K+. Overall, KF‐750 demonstrates promising potential as an adsorbent for the efficient heavy metal removal from aqueous solutions, presenting a viable option for environmental remediation.

Gold nanoparticle-mediated nanosecond laser-induced polystyrene carbonization with luminescent products

A highly soluble Au(I) gold precursor is used to produce a nanocomposite material consisting of a polystyrene matrix and gold nanoparticles. Irradiation of such a material with nanosecond laser pulses at the plasmon resonance wavelength leads to the formation of black spots containing luminescent products of carbonization. HR TEM analysis and Raman spectroscopy confirm disordered carbon. A simple model, based on laser heating of a nanoparticle to a temperature of more than 2000 K and stabilization of this temperature by the endothermic process of polystyrene carbonization, fits well with the dependence of the luminescent signal increment on the laser fluence.

Efficient adsorption of Congo red (CR) dye onto novel lignin-based magnetic core-shell adsorbent: Synthesis, characterization and experimental studies

BackgroundFurfural residue is a by-product in the furfural production from the biomass, and enriched in cellulose and lignin. Lignin is considered efficient candidates for the preparation of bio-based adsorbents because of a variety of functional groups and reactive sites involved. MethodsIn this study, we prepared the tunable covalent binding of the aldehyde-based furfural residue lignin onto amine-functionalized Fe3O4 magnetic nanoparticles using cyanuric chloride as a chemoselective cross-linker. The novel lignin-based magnetic adsorbent in core-shell structure was reported for the first time to remove Congo red from aqueous solution. Significant FindingsA distinct core-shell structure is formed, according to the SEM, TEM, FTIR, BET, XPS, and VSM techniques. Adsorption studies suggested that endothermic processes occured for CR adsorption onto AFRL@AMNP, and both pseudo-first and pseudo-second order models could provide a good description of the adsorption kinetics. The Langmuir model estimated the qmax of CR by AFRL@AMNP were 218.2 mg/g at 290 K. According to FTIR, XPS, and DFT calculations, electrostatic interactions, hydrogen bonds, and π-π interactions were identified as main mechanisms for CR onto AFRL@AMNP. More importantly, due to the incorporation of Fe3O4 magnetic nanoparticle, AFRL@AMNP can be easier to separate from the aqueous solutions and be reused.

Adsorption of amitriptyline from aqueous solutions using magnetic graphene-based material: Isotherm, kinetics, and thermodynamic study

Amitriptyline (AMT) is an antidepressant often found in water environments. Due to its toxicity, in this work, AMT adsorption was proposed using graphene oxide (GO) and magnetic GO (GO·Fe3O4 1:1). The adsorbent characterizations were accomplished by FTIR, SEM, EDS, Raman spectroscopy, XRD, and VSM revealed the typical characteristics of the pristine GO and GO·Fe3O4 1:1. In the batch adsorption study, GO·Fe3O4 1:1 showed the highest adsorption capacity (91.84 mg g−1) and removal percentage (92 %) (at pH = 9.0, C0 = 50.0 mg L−1, adsorbent dosage = 0.5 g L−1, the temperature at 293 ± 1.00 K). Moreover, the Sips model showed the best adjustment for isothermal experimental data. This model suggests that the adsorption occurs at heterogeneous surfaces when the qs value increases with the increase in temperature (from 235.57 mg g−1 at 20 ºC to 463.34 mg g−1 at 50 ºC). The thermodynamic study confirms that AMT adsorption onto GO·Fe3O4 1:1 is a spontaneous and endothermic process (ΔH = 32.75 kJ mol−1). Elovich kinetic model presented the best adjustment for experimental data and showed that the adsorption rate (α) and surface coverage constant (β), decrease with the increase of the adsorbate dosage. Additionally, the ionic strength study reveals that a high concentration of NaCl (1.0 M) decreases the qe to 25.74 mg g−1. Lastly, after five consecutive adsorption/desorption cycles, the removal percentage of GO·Fe3O4 1:1 remained elevated (79 %). Overall, this paper reports the efficiency of GO·Fe3O4 1:1 on AMT removal, in addition to investigating the several variables involved in this adsorption.

New study of the adsorption mechanism of different dye molecules by high porous sludge activated carbon produced from a dairy-treatment effluent plant

In this study, a high-quality porous sludge-activated carbon from a dairy-treatment effluent plant in México (ACSDM) was produced, characterized, and investigated in the adsorption of 8 different dyes. The main focus was establishing how the dyes' molecular characteristics affect adsorption. So, the intrinsic characteristics of the different dye molecules were correlated with the experimental adsorption data. ACSDM proved high quality, considering their textural properties and physical-chemical characteristics. Adsorption was efficient using the natural pH of each dye solution and 1 g L−1 of ACSDM. The highest adsorption capacities were obtained in the following order: Methylene Blue (MB) (998.44 mg g−1), Crystal Violet (CV) (795.65 mg g−1), Fuchsine (F) (342.52 mg g−1), Direct Blue 86 (DB-86) (306.36 mg g−1), Alizarin Green (AG) (303.25 mg g−1), Reactive Black 5 (RB-5) (259.82 mg g−1), Methanil Yellow (MY) (252.81 mg g−1) and Amaranth Red (AR) (251.12 mg g−1). These results were obtained at 55 °C (endothermic process), except for MY, where the adsorption was exothermic (25 °C). Freundlich was the model that best fitted the DB-86, MB, and CV equilibrium data. While the Langmuir and Tóth models best fit the RB-5, AR, and MY isotherms. Tóth also best represented the F and AG data. Kinetic curves demonstrated that adsorption occurred faster for dyes MB, F, CV, MY, AR, and RB-5, respectively, reaching 90 %-99 % of their saturations in the first 30 minutes. Meanwhile, the adsorption of AG and DB-86 only about 85 % of the saturation occurred. The study indicated that molecular volume is the major variable in the dye adsorption process, as well as some individual chemical characteristics of the molecule.

Influence of Lithium Triflate Salt Concentration on Structural, Thermal, Electrochemical, and Ionic Conductivity Properties of Cassava Starch Solid Biopolymer Electrolytes.

Cassava starch solid biopolymer electrolyte (SBPE) films were prepared by a thermochemical method with different concentrations of lithium triflate (LiTFT) as a dopant salt. The process began with dispersing cassava starch in water, followed by heating to facilitate gelatinization; subsequently, plasticizers and LiTFT were added at differing concentrations. The infrared spectroscopy analysis (FTIR-ATR) showed variations in the wavenumber of some characteristic bands of starch, thus evidencing the interaction between the LiTFT salt and biopolymeric matrix. The short-range crystallinity index, determined by the ratio of COH to COC bands, exhibited the highest crystallinity in the salt-free SBPEs and the lowest in the SBPEs with a concentration ratio (Xm) of 0.17. The thermogravimetric analysis demonstrated that the salt addition increased the dehydration process temperature by 5 °C. Additionally, the thermal decomposition processes were shown at lower temperatures after the addition of the LiTFT salt into the SBPEs. The differential scanning calorimetry showed that the addition of the salt affected the endothermic process related to the degradation of the packing of the starch molecules, which occurred at 70 °C in the salt-free SBPEs and at lower temperatures (2 or 3 °C less) in the films that contained the LiTFT salt at different concentrations. The cyclic voltammetry analysis of the SBPE films identified the redox processes of the glucose units in all the samples, with observed differences in peak potentials (Ep) and peak currents (Ip) across various salt concentrations. Electrochemical impedance spectroscopy was used to establish the equivalent circuit model Rf-(Cdl/(Rct-(CPE/Rre))) and determine the electrochemical parameters, revealing a higher conduction value of 2.72 × 10-3 S cm-1 for the SBPEs with Xm = 17 and a lower conduction of 5.80 × 10-4 S cm-1 in the salt-free SBPEs. It was concluded that the concentration of LiTFT salt in the cassava starch SBPE films influences their morphology and slightly reduces their thermal stability. Furthermore, the electrochemical behavior is affected in terms of variations in the redox potentials of the glucose units of the biopolymer and in their ionic conductivity.

Temperature imaging during the hydrogen release reaction from a liquid organic hydrogen carrier (LOHC) system using phosphor thermometry

Liquid organic hydrogen carrier (LOHC) systems offer a particularly interesting option for chemical hydrogen storage. In order to characterize and understand the endothermal hydrogen release from the carrier liquid and to evaluate suitable catalyst materials, knowledge of the temperature fields in the dehydrogenation reactor is important. One suitable technique for planar temperature sensing in reacting systems is phosphor thermometry. It is based on the excitation of a luminescent material by a laser pulse and detection of the subsequent phosphorescence signal. We investigated the luminescence of the thermographic phosphor (Sr,Ca)SiAIN3:Eu2+ (“SCASN:Eu2+”) dispersed in the H0-DBT / H18-DBT LOHC system in a temperature range from 400 to 600 K. A measurement cell enables repeatable and homogeneous measurement conditions of the hydrogen release reaction. A catalytic plate was put inside the heated LOHC. Temperature fields during the hydrogen release reaction were measured for the first time using the phosphorescence decay time (PDT) and the phosphorescence intensity ratio method (PIR). As expected, a strong cooling at the catalyst surface during the endothermal hydrogen release reaction could be observed, which was quantified to be in the range of 40 K.Graphical abstract

Thermodynamics, kinetic study and equilibrium isotherm analysis of cationic dye adsorption by ternary composite

This article investigates the kinetics, equilibrium, and thermodynamics of brilliant green dye adsorption on Fe3O4/CdS/MWCNTs. The effects of adsorbent dosage (0.01–0.06 g), contact time (1–120 min), temperature (278, 288,298 and 308 K), ionic strength (NaCl and CaCO3 salt), and initial solution pH (4,6,7, and 10) were all studied in relation to the adsorption of BG dye. Langmuir (R2 = 0.86883), Temkin (R2 = 0.96323) and Freundlich (R2 = 0.96958) and isotherms were fitted to describe the equilibrium of BG adsorption process. Isothermal models showed that BG adsorption was a favorable process on ternary composite Adsorption kinetics were well fitted by Pseudo-second order kinetic model (R2 = 0.99396). The thermodynamic parameters ΔH° = −0.0277 kJ.mol−1 and ΔS° = −60.9031 J mol−1.k−1 indicate endothermic and spontaneous adsorption process, (ΔG° > 0) non-spontaneous, and exothermic. Five adsorption/desorption cycles were demonstrated by the adsorbents’ high reusability.

Silica-Based 1,3-Diphenyl-1,3-Propanedione Composites: Efficient Uranium Capture for Environmental Remediation

Introduction:: This study synthesizes and characterizes a novel hybrid composite, SGdpm, to capture UO2 2+ ions from water. The composite has successfully formed by hosting covalently diphenylmethane-1,3-dione (dpm) within an inorganic silica gel matrix, showing promising potential for environmental remediation and nuclear waste management. Methods:: The preparation involved the reaction of tetraethylorthosilicate (TEOS) with diphenylmethane- 1,3-dione (dpm) under acidic conditions, resulting in white solids. The doped composite was characterized by Fourier Transform Infrared Spectroscopy (FTIR), revealing the presence of siloxane and Si-O-C bonds. The application of SG-dpm for capturing UO2 2+ ions from water was investigated, showing a shift in FTIR peaks and confirming the formation of SG-dpm-UO2 2+ as inner-sphere complexes. Scanning Electron Microscopy (SEM) revealed a non-uniform distribution of particles, essential for consistent behavior in applications such as adsorption. Results and Discussion:: Batch sorption experiments demonstrated temperature-dependent sorption behavior with increased efficiency at higher temperatures (T = 55°C). The study also explored the influence of pH and initial concentration on UO2 2+ sorption, revealing optimal conditions at pH 5 and lower initial concentrations (1.0 mg L-1). Kinetic studies using pseudo-second-order models indicated a high efficiency of UO2 2+ ion removal (99%) as a chemisorption process. Intraparticle diffusion models highlighted three distinct sorption stages. Sorption isotherm studies favored the Langmuir model, emphasizing monolayer adsorption. The thermodynamic analysis suggested an endothermic (ΔH = + 16.120 kJ mol-1) and spontaneous (ΔG = −25.113 to − 29.2449 kJ mol-1) sorption process. Selectivity studies demonstrated high efficiency in capturing Cu2+, Co2+, and Cr3+ ions, high degree selectivity of UO2 2+ ions (74%), moderate efficiency for Fe3+ and Zn2+, and lower efficiency for Pb2+, Ni2+, and Cd2+, and poor efficiency for Mn2+ ions. Conclusion: SG-dpm exhibits promising potential for selective UO2 2+ ion removal, demonstrating favorable characteristics for various applications, including environmental remediation and nuclear waste management.

MXene@polydopamine/oxidized sodium alginate modified collagen composite aerogel as sustainable bio-adsorbent for heavy metal ion adsorption and solar driven water evaporation

The design of an environmentally friendly bio-adsorbent for the removal of heavy metal ions from aqueous media is a sustainable strategy to ensure water safety. Herein, a three-dimensional macroscopic aerogel with photothermal conversion and heavy metal wastewater treatment capability was designed using leather collagen, MXene@polydopamine and oxidized sodium alginate as raw materials, named as MPAC composite aerogel. The applicability of the developed MPAC composite aerogel in water evaporation and heavy metal wastewater treatment was studied. MPAC composite aerogel had good Cr(VI) adsorption capacity. This article focused on the study of adsorption kinetics, isotherms and thermodynamics. The adsorption equilibrium time of MPAC composite aerogel was 60 min, and the equilibrium adsorption capacity of MPAC composite aerogel for Cr(VI) reached 80.73, 100.80 and 112.86 mg/g when the initial Cr(VI) concentration was 30, 70 and 100 mg/L, respectively. The adsorption process of Cr(VI) by MPAC composite aerogel conformed to the two-level dynamics model and the Freundlich adsorption isotherm model, and was a spontaneous endothermic reaction. Additionally, the composite aerogel had good solar-driven water evaporation ability and could enhance the water evaporation rate of Cr(VI) solution. Furthermore, the MPAC composite aerogel had high adsorption performance for Cr(VI) under solar illumination conditions. This new aerogel has the advantages of low cost, environmental friendliness, strong adsorption capacity and photothermal conversion performance and is a promising heavy metal ion adsorbent.

Insights into role of microstructure in TNT adsorption performances onto zeolite, diatomite and kaolinite particles

Adsorption performances of one pollutant on different adsorbents likely depend on the adsorbent microstructures heavily. Hereon, zeolite, diatomite and kaolinite particles were selected as inexpensive adsorbents in this study with 2,4,6-trinitrotoluene (TNT) as an organic pollutant for the batch test to verify the effect of adsorbent microstructure on TNT adsorption performance. The results of kinetic, adsorption isothermic, and thermodynamic analyses indicated that the adsorption process of TNT on three particles is controlled by chemisorption, and that both are non-spontaneous entropic endothermic reactions, although they have their own specific adsorption capacities, equilibration times, and kinetic rates. Comprehensively analyzing the characterization data and adsorption performances of the particles shows that, the pore physical properties including the pore diameter distribution and volume obviously control the adsorption capacities, and well the pore surface chemical properties such as the functional groups affect the adsorption kinetics; the microstructure affects the performances through the synergistic effect of physical and chemical pathways and results in the special performances. Briefly, a particle has its special microstructure and then determinedly unique performance. The finding provides insights into the role of the microstructure of the particles in their performances, and significances for selecting and utilizing the adsorbents in water treatment.

Promisingly prioritized elimination performance of europium and uranium from industrial wastewater by recyclable polydopamine functionalized hydroxyapatite/ZIF-67 hybrids

In recent decades, the nuclear industry has undergone robust growth leading to an increasingly severe issues of radionuclide contaminants in wastewater. Consequently, the development of a novel, efficient, regenerative and environmentally friendly adsorbent has become a significant challenge. In this study, recyclable polydopamine functionalized hydroxyapatite/ZIF-67 (HAP/ZIF-67/PDA) hybrids with a mass of functional groups, were successfully synthesized using the ultrasonic-assisted method. The especially characterized techniques illustrated that the HAP/ZIF-67/PDA hybrids were outstanding stable, excellent physicochemical properties and abundant functional groups. The elimination performances of Eu(III) and U(VI) from wastewater were also explored and deliberated through macroscopic experiment under diverse wastewater chemistry environment. The optimal adsorption capacity of HAP/ZIF-67/PDA was approximately 1.33 × 10-3 mol/g for Eu(III) and 8.85 × 10-4 mol/g for U(VI), surpassing those reported materials in previous literatures. The particular adsorption isotherms of Eu(III) and U(VI) were favorably fitted by Langmuir model, illustrating that the adsorption Eu(III) and U(VI) were totally endothermic reaction. The remarkable adsorption performance of HAP/ZIF-67/PDA hybrids (within 80 min for Eu(III) and 100 min for U(VI)) was verified through dynamic model, and then the kinetics results were well simulated through pseudo-second-order kinetic model, which further illustrated outstanding performance for rapidly treating Eu(III) and U(VI) under extreme emergency conditions. The primary adsorption mechanisms HAP/ZIF-67/PDA hybrids towards Eu(III) and U(VI) were surface complexation, competitive interaction, cation change, π-π* bonds and electrostatic interaction. Based on the excellent adsorption performance and recyclability of HAP/ZIF-67/PDA, it holds significantly potential and promising prospects for the efficient elimination of lanthanide and actinium contaminants from the practical treatments and disposals fields of industrial wastewater.

Efficient removal of Zn(II) ions from aqueous media using a facilely synthesized nanocomposite based on chitosan Schiff base

The development of nanomaterials incorporating organic components holds significant importance in addressing the efficient removal of metal ions through adsorption. Hence, in this study, a novel MnFe2O4/chitosan/Schiff base nanocomposite was successfully synthesized by crosslinking MnFe2O4 nanoparticles with functionalized chitosan using a novel Schiff base. The Schiff base was created through the condensation reaction between 2-aminophenol and terephthalaldehyde. Comprehensive characterization of the synthesized nanocomposite was performed through FT-IR, XRD, SEM, and VSM analyses, revealing a less crystalline arrangement compared to pure chitosan, a rough and non-uniform surface morphology, and a reduced magnetization value of 30 emu/g. Furthermore, the synthesized MnFe2O4/chitosan/Schiff base nanocomposite was working as an adsorbent for the effective disposal of Zn(II) ions from aqueous solutions. The synthesized nanocomposite exhibited a maximum sorption capacity of 289.86 mg/g for Zn(II) ions. Additionally, the results indicated that the removal of Zn(II) ions by the synthesized nanocomposite was a spontaneous, chemical, and endothermic process, aligning well with the Langmuir isotherm as well as the pseudo-second-order model. Furthermore, at pH 7.5, with a contact duration of 100 min and a temperature of 328 K, the fabricated nanocomposite reached its maximum sorption capacity for Zn(II) ions. The results of this study demonstrate the effectiveness of the newly synthesized MnFe2O4/chitosan/Schiff base nanocomposite in removing Zn(II) ions from aqueous media. The novel synthesis approach and the high adsorption capacity of 289.86 mg/g underscore the potential of this composite for practical applications in industrial wastewater treatment. The dual removal mechanism involving electrostatic attraction and complexation processes further enhances its utility, making it a valuable contribution to the field of environmental remediation.

Modeling reactive film flows down a heated fiber

We study the dynamics of an ultra-thin reactive liquid film flowing down a heated vertical fiber under the influence of gravity. A key focus is on the impact of the van der Waals attraction, which is proportional to h−3, where h denotes the film thickness. Linear stability analysis of the film flow reveals that the van der Waals attractions and the Marangoni effect enhance the instability. Furthermore, instability is reduced by exothermic chemical reactions, while it is strengthened in the case of endothermic chemical reactions. Moreover, the weakly nonlinear stability of the film flow is studied. The results indicate the possibility of both subcritical and supercritical stability in the system. Lastly, direct numerical simulations of the evolution equation are conducted for various flow parameters. These results enhance our understanding of the intricate interplay of chemical reactions, thermal effects, and intermolecular forces influencing the liquid film dynamics in complex systems.

Enhancing kaolin's structure for efficient removal of lead ions from aqueous solutions

This research demonstrates a novel methodology for structurally modifying kaolin clay to efficiently remove toxic lead ions from water through adsorption. Kaolin was systematically treated with hydrochloric acid, cetylpyridinium chloride surfactant, and calcium chloride to enhance its physico-chemical properties. BET surface area analysis, transmission electron microscopy, scanning electron microscopy, and BJH pore size measurements confirmed successful intercalation of surfactants between kaolin sheets, increasing the surface area from 43.2 to 57.1 m2 g-1 and inducing larger mesopores. Operational factors such as pH, dosage of adsorbent, time spent in contact, starting lead concentration, and temperature were tuned using batch adsorption tests. Maximum lead uptake of 29.58 mg g-1 was attained at pH 5, 20 mg adsorbent dose, 30 mg L-1 initial lead concentration, 80 min contact time, and 30°C temperature. Pseudo-second order kinetics and Sips isotherm models aptly characterized the adsorption, indicating chemisorption on heterogeneous sites. Positive enthalpy and entropy changes signified an endothermic and irreversible process. Regeneration studies demonstrated stable performance over five adsorption-desorption cycles. This comprehensive methodology integrates acid, surfactant, and cationic treatments to synthesize an eco-friendly kaolin adsorbent with enhanced selectivity and adsorption capacity for removing toxic lead from water.