Experimental Adsorption Isotherms Research Articles

Pure Hydrogen and Methane Permeation in Carbon-Based Nanoporous Membranes: Adsorption Isotherms and Permeation Experiments

Pure Hydrogen and Methane Permeation in Carbon-Based Nanoporous Membranes: Adsorption Isotherms and Permeation Experiments

Understanding the adsorption of Reactive red 2 onto metal hydroxide sludge: analysis with physico-statistical steric and energetic perspectives.

This theoretical investigation delves into the analysis of Reactive red 2 (RR-2) adsorption isotherms on metal hydroxide employing a sophisticated double-layer model characterized by dual-energy levels within the realm of physical adsorption phenomena. An examination of five distinct statistical physics frameworks was undertaken to elucidate the modeling and interpretation of equilibrium data. Expression for the physico-chemical parameters involved in the adsorption phenomena was derived based on statistical physics treatment. Fitting experimental adsorption isotherms (308-333K) to a DAMTBS has revealed the number of anchored molecules per site, occupied receptor site density, and the number of adsorbed layers. The steric parameter n varies between 0.92 and 1.05. More importantly, it is evidenced that the adhesion mechanism of (RR-2) onto metal hydroxide as determined by the estimated adsorption energies (< 40kJ/mol) supports a spontaneous and exothermic physisorption process. Thermodynamic potential functions such as entropy, Gibbs free energy, and internal energy have been computed based on the most suitable model. This research advances our physical understanding of how metal hydroxide captures dye molecules RR-2 through adsorption reaction for water depollution treatment.

Fluoride removal by hydroxyapatite modified with anhydrous aluminum chloride

ABSTRACT Efficient and low-cost removal of fluoride from water has attracted wide attention. Here, aluminum-modified hydroxyapatite (Al-HAP) was prepared by a homogeneous hydrothermal co-precipitation method. The physicochemical properties of the Al-HAP surface were characterized by SEM, XRD, FT-IR, BET, and zeta potential, and the adsorption performances were evaluated. It showed that Al-HAP has a larger specific surface area (121.97 m2/g, which is 2.3 times larger than that of HAP), more surface-active hydroxyls and positively charged at pH less than 7, which indicate that Al-HAP is beneficial to the adsorption of negatively charged fluoride. Al-HAP had a higher fluoride adsorption capacity (56.44 mg/g) than that of HAP (28.36 mg/g), and not sensitive to the interference of coexisting ions except CO32-. Based on the adsorption kinetics and adsorption isotherm experiments, the proposed two-stage kinetic model and Freundlich isotherm model can better describe the adsorption process. From the results of XPS and FT-IR, it indicated that the ion exchange between hydroxyl group on the surface and fluoride ions is the main driven force for the adsorption, and electrostatic adsorption is also helpful. The present study provides an improved HAP to effectively remove fluoride from water.

Systematic evaluation of methods for iron-impregnation of biochar and effects on arsenic in flooded soils.

There is a need for innovative strategies to decrease the mobility of metal(loids) including arsenic (As) and cadmium (Cd) in agricultural soils, including rice paddies, so as to minimize dietary exposure to these toxic elements. Iron (Fe)-modified biochars (FBCs) are used to immobilize As and Cd in soil-water systems, but there is a lack of clarity on optimal methods for preparing FBCs because there are only limited studies that directly compare BCs impregnated with Fe under different conditions. There is also a lack of information on the long-term performance of FBCs in flooded soil environments, where reductive dissolution of Fe (oxy)hydroxide phases loaded onto biochar surfaces may decrease the effectiveness of FBCs. This study uses material characterization methods including FTIR, SEM-EDX, BET, and adsorption isotherm experiments to investigate the effects of Fe-impregnation methods (pH, pyrolysis sequence, and sonication) on the morphology and mineralogy of Fe loaded onto the biochar surface, and to FBC adsorbent properties for arsenate (As(V)), arsenite (As(III)), and Cd. Acidic impregnation conditions favored the adsorption of As(III) onto amorphous Fe phases that were evenly distributed on the biochar surface, including within the biochar pore structure. The combination of sonication with acidic Fe-impregnation conditions led to the best adsorption capacities for As(V) and As(III) (4830 and 11,166 μg As g-1 biochar, respectively). Alkaline Fe-impregnation conditions led to the highest Cd adsorption capacity of 3054 μg Cd g-1 biochar, but had poor effectiveness as an As adsorbent. Amending soil with 5% (w/w) of an acid-impregnated and sonicated FBC was more effective than an alkaline-impregnated FBC or ferrihydrite in decreasing porewater As concentrations. The acid-impregnated FBC also had greater longevity, decreasing As by 54% and 56% in two flooded phases, probably due to the greater stability of Fe(III) within the biochar pore structure that may have a direct chemical bond to the biochar surface. This study demonstrates that FBCs can be designed with selectivity towards different As species or Cd and that they can maintain their effectiveness under anaerobic soil conditions. This is the first study to systematically test how impregnation conditions affect the stability of FBCs in soils under multiple drying-rewetting cycles.

New insight into CH4 adsorption mechanism in coal based on modeling analysis of different adsorption theories

Based on the principle of Gibbs excess adsorption measurement, high-pressure isothermal adsorption and desorption experiments of CH4 were performed on fractured coal samples, and CH4 adsorption phase density was obtained by the intercept method according to the experimental data. The Langmuir model, BET model, DA model, and their corrected model, the supercritical adsorption models were used for the fitting analysis of CH4 excess adsorption capacity. A hybrid model of different adsorption theories was developed based on CH4 adsorption phase density and theoretical adsorption capacity predicted by the intercept method. The transition in the occurrence pattern and control mechanism of CH4 in coal were investigated. The fitting of the Langmuir model, BET model, DA model, and their corrected models, the SBET model, the SDA model, and the SDA-L model to the CH4 excess adsorption capacity in coal shows that all multilayer adsorption theory model is not suitable for fitting the CH4 excess adsorption capacity in coal. The uncorrected Langmuir model and DA model are only suitable for fitting the CH4 excess adsorption capacity in coal in the low-pressure stage (pressure below 10MPa). The corrected Langmuir model, the corrected DA model, the SDA model, and the SDA-L model can be used to fit the CH4 excess adsorption capacity in coal, but they show some bias in predicting the theoretical CH4 adsorption capacity and the CH4 adsorption phase density. The fitting of the three main adsorption theory models suggests that there may be simultaneous monolayer adsorption and microporous filling adsorption. The fitting results of the hybrid model based on monolayer adsorption and microporous filling adsorption theory depend on showing that with the increase of temperature, the occurrence of CH4 in coal gradually changes from mainly monolayer adsorption to mainly microporous filling adsorption, and the transformation of occurrence mode is related to temperature and the development of pores in coal.

Effective removal of toxic dye from wastewater via advanced modified magnetic sepiolite using combined surfactants SDS/CTAB/Fe3O4@Sep: Empirical and computational analysis studies

In the present era, the elimination of hazardous dyes from wastewater has emerged as a paramount concern, captivating the interest of scientists globally because their detrimental effect on human health. Adsorption, a well-established and effective separation process, is commonly employed for eliminating various harmful organic pollutants from water, particularly toxic dyes. In this study, a novel magnetic organo-composite was synthesized through an environmentally friendly and easily implementable approach. Subsequently, various analytical techniques, including XRD, FT-IR, SEM, and EDX, were utilized to scrutinize the structure and morphology of the adsorbent. The as-prepared adsorbent demonstrated remarkable efficiency in rapidly removing malachite green dye from aqueous solutions, attaining a peak adsorption capacity of 227.40 mg g−1. Furthermore, several factors affecting the adsorption process were investigated, including adsorbent dosage, medium pH, initial dye concentration, and contact time. The examination of adsorption kinetics data indicated that the process adhered to a pseudo-second-order model (R2 = 0.97), implying that chemisorption constituted the controlling step in the reaction. Additionally, the experimental adsorption isotherms exhibited a close fit to the Langmuir model (R2 = 0.98). Crucially, the SDS/CTAB/Fe3O4@Sep magnetic organo-nanocomposite adsorbent exhibited the capacity for multiple reuses, maintaining its effectiveness over five cycles without notable activity decline. Consequently, the synthesized organo-composite appears to show potential as an effective adsorbent for eliminating harmful cationic dyes present in wastewater. Molecular dynamics (MD) simulations, employing Monte Carlo adsorption locator simulation (MCL) calculations, further supported the elevated adsorption of SDS/CTAB on Sep, Fe3O4 on SDS/CTAB@Sep, and MG molecules on SDS/CTAB/Fe3O4@Sep due to their negative adsorptions.

A study on the performance of a recyclable adsorbent La@Fe for phosphate adsorption in wastewater

Phosphorus(P) is the key element of the growth of phytoplankton, and is also significant cause of water eutrophication. In this work, the magnetic Fe3O4 (FE) microspheres were employed as the core material, the La compound was coated on the surface of the FE microspheres and the adsorbent obtained was denoted as La@Fe. The effects of preparation conditions including the dosage of NaOH, the preparation time, the ratio of FE and LaCl3 (LC), and the stirring time were discussed. The optimized La@Fe has a good adsorption capacity (130-160mg·g-1) and strong magnetic recovery capacity (43.4emu/g). In the low concentration (1mg·L-1), the optimized La@Fe still had an excellent performance. It can keep a good adsorption in a wide pH range (3-8). Except Na2CO3, common anions (NaHCO3, NaCl, NaNO3, Na2SO4, KF, KNO2) in the wastewater could not affect the adsorption capacity of La@Fe. After 7 regeneration, the adsorption capacity of La@Fe reduced by 25% indicating the excellent regeneration property of La@Fe. The La@Fe was analyzed by SEM, TEM, XRD, XPS, BET, and LPS, and the obtained results showed that the particles of La@Fe were spherical, the particle sizes were between 0.1 and 100μm. The main components at the surface of La@Fe was La-(OH), which adsorbed phosphate to form La-PO4. The specific surface area of La@Fe was small and the mesopores were main pore structure. In addition, the adsorption kinetics analysis indicated that the Elovich model worked well on modeling La@Fe adsorbing phosphate, so the adsorption was chemical adsorption with heterogeneous adsorbing surfaces. Adsorption isotherms experiments revealed that the increasing adsorption temperature would enhance the adsorption capacity of La@Fe. It could be obtained from the thermodynamic experiments that the adsorption process was endothermic and chemical adsorption. Therefore, La@Fe is an excellent phosphate adsorbent and has a good application prospect in the field of phosphorus recovery and adsorbent reuse.

Density and volume of adsorbed methane in key applications for in-situ gas content: Insights from molecular simulation

The evaluation of the in-situ gas content in deep coal seams, potentially containing free gas in saturated-oversaturated reservoirs, holds practical significance for exploration and production compared with shallow undersaturated-saturated reservoirs dominated by adsorbed gas. However, owing to the inherent limitations of volumetric and gravimetric methods, the accurate assessment of adsorbed and free gases faces significant challenges. In this study, based on molecular simulations, we focused on slit-shaped pores to explore the microscopic interaction mechanisms between coal and methane molecules under different pore sizes, temperatures, and pressures. By combining isothermal adsorption and pore structure experiments, the distribution characteristics of the adsorbed phase density (APD) and adsorbed phase volume (APV) were determined. The results showed that, in pores smaller than 1.5 nm, methane exhibited an aggregated state distribution (containing only adsorbed methane) characterized by micropore filling adsorption. In pores larger than 1.5 nm, methane showed a dispersed state distribution (coexistence of adsorbed and free methane) characterized by monolayer adsorption. The APD increased with pressure and decreased with temperature and pore size, whereas the APV remained independent of the pressure and temperature. In the in-situ gas content evaluation, three adsorption models (SL, SDR, and SL + SDR models) considering APV and APD were utilized to describe the methane adsorption behavior. The SDR model considering the APV was consistent with the actual physical properties and molecular simulation results. Traditional correction methods often lead to an overestimation of the adsorbed methane content, and neglecting the APV can result in an overestimation of the free methane content. In summary, the SDR model considering the APV can provide more rigorous scientific support for the refined study of methane occurrence states and gas content distribution.

Structural and Vibrational Properties of Carboxylates Intercalated into Layered Double Hydroxides: A Joint Computational and Experimental Study.

Layered double hydroxides (LDHs) are fascinating clay-like materials that display versatile properties, making them an extremely fertile playground for diverse applications, ranging from bio-compatible materials to the pharmaceutical industry to catalysis and photocatalysis. When intercalating organic and bio-organic species between the inorganic layers, such materials are named hybrid LDHs. The structure-property relation in these systems is particularly relevant, since most of the properties of the materials may be fine-tuned if a comprehensive understanding of the microscopic structure in the interlamellar space is achieved, especially with respect to the reorganization under water uptake (swelling). In this work, we combined experiments and simulations to rationalize the behavior of LDHs intercalating three carboxylates, the general structure of which can be given as [Mg4Al2(OH)12]A2-·XH2O (with A2- = succinate, aspartate, or glutamate and X representing increasing water content). Following this strategy, we were able to provide an interpretation of the different shapes observed for the experimental water adsorption isotherms and for the evolution of the infrared carboxylate band of the anions. Apart from small differences, due to the different reorganization of the conformational space under confinement, the behavior of the two amino acids is very similar. However, such behavior is quite different in the case of succinate. We were able to describe the different response of the anions, which has a significant impact on the isotherm and on the size of the interlamellar region, in terms of a different interaction mechanism with the inorganic layer.

Synthesis of porous carbon/zeolite composites by low-temperature acid-alkaline leaching from coal gasification fine slag for adsorption of dye wastewater

The conversion and utilization of coal gasification slag is considered one of the key issues in the development of the modern coal chemical industry. In this work, porous carbon/Na-P1 zeolite composites were successfully prepared by a simple and easy-to-operate acid-alkali leaching method on the basis of the composition of coal gasification fine slag. The synthesized CZ-10 possessed a honeycomb-like porous carbon structure and a typical flower-cluster zeolite structure, with the specific surface area and pore volume reaching 195.68 m2/g and 0.257 m3/g, respectively. CZ-10 showed excellent adsorption performance, with an equilibrium adsorption capacity of 175.93 mg/g on methylene blue (MB) at 300 K. CZ-10 can effectively adsorb MB in a wide pH range, and the increase in pH was favorable for adsorption. According to the results of adsorption kinetics and isothermal adsorption experiments, the adsorption process was in good agreement with PSO model and Sips model. According to the characterization results and adsorption experiments, it was speculated that the adsorption of CZ-10 on MB was mainly chemisorption, and may be affected by various factors such as ion-exchange, electrostatic attraction, hydrogen bonding, π-π bonding and van der Waals forces.

Cyclodextrin-Assisted Surface-Enhanced Photochromic Phenomena of Tungsten(VI) Oxide Nanoparticles for Label-Free Colorimetric Detection of Phenylalanine.

Herein are presented the results of experiments designed to evaluate the effectiveness of host-guest interactions in improving the sensitivity of colorimetric detection based on surface-enhanced photochromic phenomena of tungsten(VI) oxide (WO3) nanocolloid particles. The UV-induced photochromic coloration of WO3 nanocolloid particles in the presence of aromatic α-amino acid (AA), l-phenylalanine (Phe) or l-2-phenylglycine (Phg), and heptakis(2,3,6-tri-O-methyl)-β-cyclodextrin (TMβCDx) in an aqueous system was investigated using UV-vis absorption spectrometry. The characteristics of the adsorption modes and configurations of AAs on the WO3 surface have also been identified by using a combination of adsorption isotherm analysis and attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR). A distinct linear relationship was observed between the concentration of AAs adsorbed on the WO3 nanocolloid particles and the initial photochromic coloration rate in the corresponding UV-irradiated colloidal WO3 in aqueous media, indicating that a simple and sensitive quantification of AAs can be achieved from UV-induced WO3 photochromic coloration without any complicated preprocessing. The proposed colorimetric assay in the Phe/TMβCDx/WO3 ternary aqueous system had a linear range of 1 × 10-8 to 1 × 10-4 mol dm-3 for Phe detection, with a limit of detection of 8.3 × 10-9 mol dm-3. The combined results from UV-vis absorption, ATR-FTIR, and adsorption isotherm experiments conclusively indicated that the TMβCDx-complexed Phe molecules in the Phe/TMβCDx/WO3 ternary aqueous system are preferentially and strongly inner-sphere adsorbed on the WO3 surface, resulting in a more significant surface-enhanced photochromic phenomenon. The findings in this study provided intriguing insights into the design and development of the "label-free" colorimetric assay system based on the surface-enhanced photochromic phenomenon of the WO3 nanocolloid probe.

Measurement of elements by portable x-ray fluorescence spectrometry for the study of adsorption processes: the case of Pb2+ adsorption on soybean straw biochar

This study evaluated the reliability of portable X-ray fluorescence (pXRF) in Pb2+ adsorption kinetics and isotherm experiments using soybean straw biochar. The research aimed to compare pXRF results with those obtained through traditional atomic absorption spectrometry (AAS). Soybean straw biochar, produced at 400 °C, was employed as the adsorbent for Pb2+. The efficiency of adsorption was assessed using Langmuir and Freundlich models. The kinetics of Pb2+ adsorption was analysed through pseudo-first-order and pseudo-second-order models. The pseudo-second-order model described the kinetics of Pb2+ adsorption on biochar better than the pseudo-first order model. Importantly, the pXRF technique demonstrated comparable results to those of AAS, making it a reliable and resource-efficient method for studying Pb2+ kinetics. The results of the isotherm analyses fit the Langmuir model, indicating a desirable and irreversible adsorption of Pb2+ on biochar. PXRF measurements on biochar allowed simultaneous observations of Pb2+ adsorption and K+ and Ca2+ desorption, highlighting ionic exchange as the primary adsorption mechanism. In conclusion, our results showcased the applicability of pXRF for Pb+2 adsorption studies in biochars, offering a valuable alternative to traditional methods. The findings contribute to the understanding of biochar as an effective adsorbent for heavy metals, emphasizing the potential of pXRF for cost-effective and efficient environmental research. In this study, we present a novel and detailed procedure that will allow other researchers to continue their studies on Pb2+ adsorption on biochar or similar matrices, significantly reducing the resources and time used and enabling the simultaneous study of the behavior of other ions participating in the process.

Experimental and numerical study of hydrogen adsorption by the Ni0.6Mg0.4Fe2O4 compound

This paper proposes an experimental and numerical study of the hydrogen storage properties of the Ni0.6Mg0.4Fe2O4 compound. Firstly, the sol-gel method was used to synthesize the compound Ni0.6Mg0.4Fe2O4. Second, the synthesized compound's morphological and structural properties were ascertained using X-ray and SEM techniques. Third, the experimental hydrogen adsorption's kinetics and isotherms were carried out. At last, the experimental hydrogen adsorption isotherms were compared to a mathematical model based on the formalism of statistical physics. With the use of this model, it was possible to ascertain the following: on the one hand, the stereographic parameters involved in the adsorption process, such as the number of receptor sites (n1 and n2), their density (Nm1 and Nm2), as well as the energy parameters (P1 and P2) and the energies of adsorption for each type of site (ΔEads1 and ΔEads2). On the other hand, the thermodynamic functions that regulate the hydrogen adsorption reaction, such as the internal and Gibbs energies, as well as the entropy versus temperature and pressure. Ni0.6Mg0.4Fe2O4 has a significant hydrogen storage capacity (0.15 wt %) at moderate temperatures. The numerical results showed that hydrogen is inserted into two types of interstitial sites via an exothermic process.

Functionalized activated carbon with whey protein amyloid fibrils for adsorption of arsenic from water

Globally, more than 200 million people are exposed to elevated concentrations of arsenic in groundwater, thus representing an important environmental and public health problem. Apart from inorganic species, water quality suffers also from the occurrence of organic pollutants discharged by the food sector like whey, a by-product of the dairy industry. The valorisation of these organic residues is relevant to reduce water pollution and to develop new materials for different applications. This research reports the synthesis and evaluation of a novel adsorptive activated carbon composite modified with whey protein amyloids for arsenic removal from water. The adsorbent was characterized with FT-IR spectroscopy, X-ray diffraction, N2 physisorption, pH at point of zero charge determination, and thermogravimetric analysis. Experimental adsorption kinetics and isotherms of arsenic removal were determined at optimal pH 5.0, best fitted with the PSO and Sips model, respectively. The corresponding maximum adsorption capacity for As5+ was 0.16 mmol g−1 through an endothermic process. Surface complexation was the predominant phenomenon in the adsorption mechanism as the As-O bond was formed via whey’s functional groups, hydroxyl, amine, and amide, with the latter having the strong affinity to arsenate as elucidated by the HSAB theory. This study highlights the potential of whey protein as a raw material to produce added-value products and its performance as a precursor of novel adsorbents for water purification, therefore minimizing their associated disposal cost and addressing relevant environmental concerns such as arsenic contamination.

Reservoir Characteristics of the Main Coal Seams in the Longtan Formation, Guxu Coal Mining Area, Sichuan

To facilitate the efficient exploration and development of coalbed methane of the Longtan Formation in the Guxu coal mining area, Sichuan, it is essential to evaluate the reservoir characteristics of the main production layers. In this study, scanning electron microscopy, low-temperature liquid nitrogen adsorption experiments, high-pressure mercury pressure experiments, and isothermal adsorption experiments were conducted to investigate the reservoir characteristics of favorable coalbed methane reservoirs. The results indicate that the main coal seams in the Longtan Formation are medium-to-high ash content anthracite with a well-developed pore–fracture system. The pore size distribution exhibits both unimodal and bimodal types, while the pore morphology includes impermeable pores closed at one end, open permeable pores, and ink bottle-shaped pores. It shows that the middle part of Longtan Formation acts as an enrichment zone for coalbed methane, which is characterized by a stronger adsorption capacity, high Langmuir volume, high gas content, and high gas saturation distribution. The pH value, mineralization degree, and hydrogen–oxygen isotope of the produced water in the main coal seams indicate that the enrichment zone is typically located in a stagnant flow zone with a reducing environment and favorable storage conditions.

Anionic Dye Removal with a Thin Cationic Polyaniline Coating on Cellulosic Biomaterial.

This paper reports the development of novel adsorbent materials using polyaniline (PANI) grafted onto Posidonia (POS) fibers, aimed at efficiently removing phenol red (PSP), an anionic dye, from aqueous solutions. The synthesis involved the copolymerization of aniline grafted on the surface of the POS and aniline monomer in solution, resulting in a chemically bound thin PANI layer on the POS bioadsorbent. Structural characteristics and binding affinities of these adsorbents with PANI under its emeraldine salt (POS@PANI-ES) or emeraldine base (POS@PANI-EB) forms are reported. The rapid adsorption kinetics observed are attributed to enhanced accessibility to PANI adsorption sites on the POS surface. The binding percentages of PSP to POS@PANI-ES and POS@PANI-EB materials were found to be 97 and 50%, respectively, after 15 min of contact time. The Langmuir model for localized adsorption sites and the Volmer model for nonlocalized adsorption as a mobile layer were fitted to the experimental adsorption isotherms of PSP to POS@PANI-EB and POS@PANI-ES, yielding the thermodynamic parameters of adsorption. The adsorption capacities of PSP on POS@PANI-EB and POS@PANI-ES were 37.8 and 71.5 μmol g-1, respectively. The adsorption of PSP remained above 80% at moderate salt concentrations of around 0.1 mol L-1; however, higher concentrations of NaCl and CaCl2 in PSP solutions significantly reduced the adsorption on POS@PANI-ES.

Migration characteristics of constant elements in the process of coal dissolution by liquid CO2

The effect of liquid CO2 on coal dissolution plays a key role in improving coal bed methane (CBM) recovery and CO2 geological storage. In order to study the effect of liquid CO2–H2O reaction on the migration of mineral constant elements in coal, three kinds of coal samples (lignite, bituminous coal, and anthracite) with different degrees of metamorphism were selected as the research objects. The one-factor experiments of dissolution of liquid CO2 and water-bearing coal samples were carried out by simulating the temperature and pressure of the stratum. X-ray fluorescence spectroscopy (XRF) was used to test the changes in the relative content of constant elements in coal samples after liquid CO2 injection under different pressure conditions. Scanning electron microscopy (SEM) was utilized to observe the evolution pattern of the surface features of the coal before and after the dissolution of liquid CO2. A quantitative analysis of coal pore development characteristics was conducted based on low-temperature N2 adsorption/desorption experiments, and isothermal adsorption experiments were carried out before and after etching the coal samples to understand the adsorption characteristics of CH4 and CO2 by coal under different pressure conditions. The research results indicated that the migration ability of constant elements in coal showed a trend of first decreasing and then increasing with the increasing degree of coal metamorphism. Among the three selected coal samples, the migration ability of constant elements was found to be strongest in anthracite, followed by lignite and bituminous coal. Most of the element migration in coal was carried out through chemical reactions (hydrolysis, carbonation, redox), while some elements were primarily transported through physical means (such as the low-temperature impact of liquid CO2). The dissolution process expands the original pore space of coal and generates new pores, greatly increasing the coal's capacity for CO2 adsorption. These findings deepen our understanding of mineral dissolution in coal by liquid CO2 and provide important insights for achieving efficient and long-term coalbed CO2 geological storage and enhanced methane recovery techniques.

Differential Analysis of Various Moisture Phases on N2 Displacement of CH4 in Coal.

The aim of the study was to elucidate the impact of different moisture phases during gas injection on coalbed methane displacement. The coal samples were treated with two methods: water vapor adsorption and liquid water stirring. The differences in the coal samples treated with various moisture phases during gas injection for coalbed methane displacement were investigated by using the isothermal adsorption curves of CH4, N2, and H2O in coal and N2 displacement of CH4 in coal. The results indicate that variations in the gas adsorption capacity of coal are treated with different moisture phases. The gas adsorption capacities and displacement capacities of the coal samples treated with the water vapor adsorption methods are better than those treated with the stirring methods. In the isothermal adsorption experiment, for the coal samples treated with different moisture phases, at a moisture content of 2.75%, the saturated adsorption capacities of CH4/N2 are 0.204/0.189 (cm3/g), and at a moisture content of 5.63%, the saturated adsorption capacities of CH4/N2 are 0.151/0.139 (cm3/g). In addition, in the displacement experiment, for the coal samples treated with different moisture phases, at a moisture content of 2.75%, the difference in the total gas adsorption capacities is 0.62 cm3/g and the difference in the CH4 adsorption capacities is 0.473 cm3/g, and at a moisture content of 5.63%, the difference in the total gas adsorption capacities is 0.3 cm3/g and the difference in CH4 adsorption capacities is 0.22 cm3/g. For the coal samples treated with various moisture phases, the differences in the CH4/N2 adsorption and displacement capacities are greater at a moisture content of 2.75% than at 5.63%. Notably, the moisture phase has only a marginal influence on the CH4 desorption capacity and desorption rate. The study is important to understand the interactions between coal and moisture.

Bio-sorption capacity of cadmium and zinc by Pseudomonas monteilii with heavy-metal resistance isolated from the compost of pig manure

The tolerance of Pseudomonas monteilii X1, isolated from pig manure compost, to Cd and Zn, as well as its capacity for biosorption, were investigated. The minimum inhibitory concentrations (MIC) of Cd and Zn for the strain were 550 mg/L and 800 mg/L, respectively. Untargeted metabolomics analysis revealed that organic acids and derivatives, lipids and lipid-like molecules, and organic heterocyclic compounds were the main metabolites. The glyoxylate and dicarboxylate metabolism pathway were significantly enriched under Cd2+ stress. The isothermal adsorption and adsorption kinetics experiments determined that the strain had adsorption capacities of 9.96 mg/g for Cd2+ and 23.4 mg/g for Zn2+. Active groups, such as hydroxyl, carboxyl, and amino groups on the cell surface, were found to participate in metal adsorption. The strain was able to convert Zn2+ into Zn3(PO4)2·4H2O crystal. Overall, this study suggested that Pseudomonas monteilii has potential as a remediation material for heavy metals.

Detection and adsorption of 2-methyl-4-chlorophenoxyacetic acid in vegetables via dual-functional molecularly imprinted polymer doping with carbon dot

2-Methyl-4-chlorophenoxyacetic acid (MCPA) is one of the most widely used herbicides, so adsorption and detection of MCPA in the environment is critical. Blue fluorescent carbon dot (CD) was synthesized from citric acid and urea, which could be quenched by MCPA. Herein, bifunctional molecularly imprinted polymer (CD@MIP) was prepared on monodisperse poly (glycidyl methacrylate-co-ethylene glycol dimethacrylate) microspheres, with 4-vinylpyridine as the functional monomer, ethylene glycol dimethacrylate as the cross-linking agent, and doped with CD. The enrichment ability of CD@MIP for MCPA and fluorescence detection performance were determined. The maximum adsorption amount of MCPA was 93.9 mg g−1 as determined by isothermal adsorption experiments and was in accordance with the Langmuir adsorption model. The results of the kinetic experiments showed that the adsorption equilibrium reached within 30 min, which possessed a relatively fast adsorption rate and was in accordance with the pseudo-second-order adsorption model. Both MIP without CD and non-imprinted polymers were also fabricated and tested as references. Fluorescence experiments showed good linearity of CD@MIP in the range of 0–80 μmol. The cabbage samples were analyzed by high performance liquid chromatography with a linear range of 0.02–15 μg mL−1, recoveries of 90.5%–98% and low relative standard deviations (RSD, n = 3) of 1.5%–5.9%. CD@MIP with excellent performance provides a feasible practical application in the detection and enrichment of MCPA.