Dynamic Adsorption Experiments Research Articles

Study on the adsorption mechanism of fluorescent nano-tracer in sandstone core

Chemical tracer testing technology has increasingly become the preferred method for reservoir monitoring in oil fields due to its low cost and high efficiency. Understanding the migration behavior and adsorption mechanisms of chemical tracers in porous media is crucial for designing tracer injection processes and enhancing the accuracy of tracer test interpretation. This study employs an enhanced Stöber sol-gel method to synthesize fluorescent silica nanoparticles. After surface modification with the silane coupling agent γ-(methacryloyloxy) propyltrimethoxysilane (KH570) and doping with two fluorescent dyes, a multicolor fluorescent nano-tracer (PMFN) was synthesized. This study conducted dynamic and equilibrium adsorption experiments to investigate the adsorption behavior of PMFN on sandstone surfaces. To elucidate the adsorption mechanism of PMFN, we fitted the adsorption equilibrium experimental data using the Langmuir, Freundlich, and Temkin isothermal adsorption models. The adsorption kinetics were studied using the Lagergren, Elovich, and pseudo-first-order kinetic models. Additionally, we assessed the influence of ionic strength and particle size on the adsorption of PMFN by calculating the DLVO interaction forces between PMFN and the sandstone surface. The results showed that PMFN adsorption on sandstone primarily occurs in the pre-contact stage and is characterized by monolayer adsorption. When the ionic strength of the solution is 0.001 mol/L, the maximum repulsive energy barrier between PMFN and the sandstone surface hinders adsorption.

Sodium Alginate/UiO-66-NH2 Nanocomposite for Phosphate Removal.

Environmental pollution of phosphorus is becoming increasingly concerning, and phosphate removal from water has become an important issue for controlling eutrophication. Modified metal-organic framework (MOF) materials, such as UiO-66-NH2, are promising adsorbents for phosphate removal in aquatic environments due to their high specific surface area, high porosity, and open active metal sites. In this study, a millimeter-sized alginate/UiO-66-NH2 composite hydrogel modified by polyethyleneimine (UiO-66-NH2/SA@PEI) was prepared. The entrapping of UiO-66-NH2 in the alginate microspheres and its modification with PEI facilitate easy separation in addition to enhanced adsorption properties. The materials were characterized by SEM, FTIR, XRD, and BET. Static, dynamic, and cyclic adsorption experiments were conducted under different pH, temperature, adsorbent dosage, and initial concentration conditions to assess the phosphate adsorption ability of UiO-66-NH2/SA@PEI. Under optimal conditions of 65 °C and pH = 2, 0.05 g UiO-66-NH2/SA@PEI adsorbed 68.75 mg/g, and the adsorption rate remained at 99% after five cycles of UiO-66-NH2/SA@PEI. These results suggest that UiO-66-NH2/SA@PEI composite materials can be used as an effective adsorbent for phosphate removal from wastewater.

Preparation of 6-Amino-N-hydroxyhexanamide-Modified Porous Chelating Resin for Adsorption of Heavy Metal Ions.

The pollution of water bodies by heavy metal ions has recently become a global concern. In this experiment, a novel chelating resin, D851-6-AHHA, was synthesized by grafting 6-amino-N-hydroxyhexanamide (6-AHHA) onto the (-CH2N-(CH2COOH)2) group of the D851 resin, which contained a hydroxamic acid group, amide group, and some carboxyl groups. This resin was developed for the purpose of removing heavy metal ions, such as Cr(III) and Pb(II), from water. The findings from static adsorption experiments demonstrated the remarkable adsorption effectiveness of D851-6-AHHA resin towards Cr(III) and Pb(II). Specifically, the maximum adsorption capacities for Cr(III) and Pb(II) were determined to be 91.50 mg/g and 611.92 mg/g, respectively. Furthermore, the adsorption kinetics of heavy metal ions by D851-6-AHHA resin followed the quasi-second-order kinetic model, while the adsorption isotherms followed the Langmuir model. These findings suggest that the adsorption process was characterized by monolayer chemisorption. The adsorption mechanism of D851-6-AHHA resin was comprehensively investigated through SEM, XRD, FT-IR, and XPS analyses, revealing a high efficiency of D851-6-AHHA resin in adsorbing Cr(III) and Pb(II). Specifically, the (-C(=O)NHOH) group exhibited a notable affinity for Cr(III) and Pb(II), forming stable multi-elemental ring structures with them. Additionally, dynamic adsorption experiments conducted using fixed-bed setups further validated the effectiveness of D851-6-AHHA resin in removing heavy metal ions from aqueous solutions. In conclusion, the experimental findings underscored the efficacy of D851-6-AHHA resin as a highly efficient adsorbent for remediating water bodies contaminated by heavy metal ions.

Construction of hydrophobic ALF@poly(acrylates)-F composite for dynamic adsorption of CO2 from humid flue gas

The combustion of fossil fuels leads to significant CO2 emissions. The cost-effective Al(HCOO)3 (ALF) demonstrates exceptional CO2 adsorption capacity, while its powder form and poor stability in humid flue gas challenge for practical application. In this study, we explored a strategy that combines a hydrophobic and well-knit matrix with high-performance and affordable CO2 adsorbent, further hydrophobic coating was carried out on the composite. This methodology achieved a high loading (72.3 wt%) of uniformly ordered carbophilic and hydrophobic ALF@poly(acrylates)-F composite beads that had approximately one-third smaller in size and the unit crystal adsorption efficiency 1.45 times higher at 1 bar compared to ALF powder. Furthermore, the composite exhibited faster kinetics and excellent CO2/N2 selectivity (307, 298 K). Notably, the multi-component dynamic adsorption experiments showed that ALF@poly(acrylates)-F composite with hydrophobic coating maintained 99.1 % of its dry CO2 adsorption capacity in the simulated wet flue gas (15 CO2 vol%/85 N2 vol%, 80 % RH).

Mixed‐charge cellulose nanocrystal modified cellulose acetate membrane with endotoxin scavenging ability and antibacterial properties

AbstractBlending modification is used to improve the hemocompatibility of cellulose acetate (CA) dialysis membranes while endowing the CA membrane with endotoxin scavenging and antibacterial capabilities. First, polydopamine (PDA) and polyethylenimine (PEI) are used as negatively charged and positively charged moieties, respectively, together with cellulose nanocrystals (CNCs) to construct mixed charge CNCs (PEI‐PDA@CNCs). Then PEI‐PDA@CNCs is blended with the CA casting solution, and the modified CA dialysis membrane is prepared through a phase inversion process. Through biocompatibility, adsorption, antibacterial, and filtration experiments, various properties of PEI‐PDA@CNCs modified CA membrane (PDCA) are systematically tested. The results show that the PDCA membrane exhibited good blood compatibility and noncytotoxicity. At the same time, the PDCA membrane has antibacterial properties and excellent endotoxin adsorption capacity. Compared with the CA membrane, the clearance rates of PDCA membrane for Staphylococcus aureus and Escherichia coli reach 54.0% ± 1.5% and 52.9% ± 5.9% respectively. In the dynamic adsorption experiment, the adsorption capacity of PDCA membrane for endotoxin increases to 2322.1 ± 45.9 EU/g. The research results indicate that PEI‐PDA@CNC‐modified multifunctional CA membrane with endotoxin adsorption and antibacterial properties has potential application prospects in the fields of hemodialysis and blood purification.

Study on adsorption and purification materials for ethylene in cold storage

In view of the lack of systematic quantitative and comparative studies on the purification effect of ethylene adsorbent in cold storage, starting from the selection of purification materials, this paper analyzed the purification effect of different zeolite materials on ethylene through a small test chamber, and screened out the best zeolite adsorbents used in self-made purification device. Combined with characterization analysis, purification efficiency evaluation and adsorption capacity of zeolite material, the removal performance of ethylene was investigated. The results showed that the zeolite samples with rough and porous surface showed better adsorption performance for ethylene. The larger the specific surface area and total pore volume, the stronger the adsorption capacity to ethylene. In addition, the presence of Na elements and mesoporous increased the exchange capacity and pore volume, which also played a certain role in the ethylene adsorption process. Experimental result demonstrates that clean air volume (CADR) of ethylene is 232 m3/h, the ethylene removal rate at 30 min is 98.19%, and the purification energy efficiency is 1.39. At the same time, the adsorption capacity of the selected zeolite sample is 1380.5 μg/g by dynamic adsorption experiment, and the service life of the filter element of the self-made purification device is estimated to be 166 days. This study can provide a theoretical basis for ethylene purification in cold storage.

Graphene Oxide/Polyamidoamine G4 as a High Efficient and Eco-Friendly Adsorbent for Dichromate Ions.

In this study, GO/PAMAM4 was used as a biocompatible nanocomposite adsorbent to adsorb dichromate (DC) ions. In alkaline solutions, DC ions changed to chromate ions which were not adsorbed on the surface of adsorbent. Thus, experiments were carried out in acidic and neutral water solution. Under these conditions, adsorption sites of adsorbent were protonated primary and ternary amine groups of adsorbent shown as -NH3+ and -NHR2+, respectively, that adsorbed DC ions through electrostatic interaction. Adsorption isotherms of DC on GO/PAMAM4 were obtained under various ionic strengths, pHs and temperatures. Isotherms were analyzed by the ARIAN model. The highest observed adsorption capacity of this process was 246.7 mg g-1 at pH=0 and 318 K. Tests at pH=2 showed that this process was endothermic. Adsorption kinetic experiments were carried out under various initial DC concentrations, pHs, temperatures, shaking rates and ionic strengths and were analyzed by the KASRA model and intraparticle diffusion, ISO and NIPPON equations. Pb2+, Cd2+, Cr3+ and tannic acid (TA) were separated by GO/PAMAM4 from DC ions and the GO/PAMAM4 was recycled by using an alkaline solution.

Study on Adsorption of Cd in Solution and Soil by Modified Biochar-Calcium Alginate Hydrogel.

Contamination with cadmium (Cd) is a prominent issue in agricultural non-point source pollution in China. With the deposition and activation of numerous Cd metal elements in farmland, the problem of excessive pollution of agricultural produce can no longer be disregarded. Considering the issue of Cd pollution in farmland, this study proposes the utilization of cross-linked modified biochar (prepared from pine wood) and calcium alginate hydrogels to fabricate a composite material which is called MB-CA for short. The aim is to investigate the adsorption and passivation mechanism of soil Cd by this innovative composite. The MB-CA exhibits a higher heavy metal adsorption capacity compared to traditional biochar and hydrogel due to its increased oxygen-containing functional groups and heavy metal adsorption sites. In the Cd solution adsorption experiment, the highest Cd2+ removal rate reached 85.48%. In addition, it was found that the material also has an excellent pH improvement effect. Through the adsorption kinetics experiment and the soil culture experiments, it was determined that MB-CA adheres to the quasi-second-order kinetic model and is capable of adsorbing 35.94% of Cd2+ in soil. This study validates the efficacy of MB-CA in the adsorption and passivation of Cd in soil, offering a novel approach for managing Cd-contaminated cultivated land.

Removal of Pb pollution using alginate-coupled magnetic sludge biochar: Solidification and stabilization behavior and electron promotion mechanisms

Environmental and human health problems caused by Pb pollution have attracted much attention, and solidification and stabilization are effective means for its remediation. Improving the ability of biochar to remediate heavy metals through modification is the focus of current biochar research. This study used calcium-alginate gel (GB) and Fe3+ (magnetic) to encapsulate and improve sludge biochar (SB), and explored the adsorption behavior and passivation mechanism of Pb2+ on it from outside to inside. The magnetic-biochar (MB) in magnetic-biochar-gel microspheres (MBGB) showed a homogeneous dispersion and part of the Fe ion was detached from the MB into the three-dimensional pores of the gel. The results of kinetic, isothermal and pH adsorption experiments showed that the MBGB has 108.4 % and 200 % higher Pb2+ adsorption capacity and rate than SB and can be applied to pH 3–9. The adsorption of Pb2+ by MBGB is a multilayer adsorption with both physical and chemical mechanisms. Mineralogical and electrochemical results demonstrate that the cross-linking of the gel with magnetic-biochar (MB) can provide a directional diffusion channel for Pb2+ from the outside to the inside. The electron transfer rate of MBGB was significantly higher than that of SB (222.2 %) after the reaction. The dissolved cations and electrons on the MB guide Pb2+ from the MBGB surface to the internal MB quickly via accelerating the electron transfer and migration rate between Pb2+ and MB. Subsequently, the abundance of PO43− on the MB ensures stable mineral precipitation (Pyromorphite). Moreover, four-step extraction analysis confirmed that most of Pb2+ in MBGB was stable (36.2 % acid-soluble and 47.6 % non-bioavailable). Meanwhile, the Pb adsorption efficiency of MBGB was still >93.0 % after three cycles of adsorption-desorption. Excellent reuse performance and stability guarantee the environmental security of MBGB. The results of the study provide theoretical support for the efficient treatment of Pb2+ polluted water assisted by gel materials.

Synthesis and Characterization of Boronate Affinity Three-Dimensionally Ordered Macroporous Materials.

Sample pretreatment is a key step for qualitative and quantitative analysis of trace substances in complex samples. Cis-dihydroxyl (cis-diol) group-containing substances exist widely in biological samples and can be selectively bound by boronate affinity adsorbents. Based on this, in this article, we proposed a simple method for the preparation of novel spherical three-dimensionally ordered macropore (3DOM) materials based on a combination of the boronate affinity technique and colloidal crystal template method. The prepared 3DOM materials were characterized using Fourier transform-infrared spectroscopy, scanning electron microscopy, X-ray photoelectron spectroscopy, and thermo-gravimetric analysis, and results showed that they possessed the characteristics of a high specific surface area, high porosity, and more boronic acid recognition sites. The adsorption performance evaluation results showed that the maximum adsorption capacity of the boron affinity 3DOMs on ovalbumin (OVA) could reach to 438.79 mg/g. Kinetic and isothermal adsorption experiments indicated that the boronate affinity 3DOM material exhibited a high affinity and selectivity towards OVA and adenosine. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis of the proteins in egg whites was conducted and proved that the glycoprotein in the egg whites could be separated and enriched with a good performance. Therefore, a novel boronate affinity 3DOM material a with highly ordered and interconnected pore structure was prepared and could be applied in the separation and enrichment of molecules with cis-diol groups from complex samples with a good selectivity, efficiency, and high throughput.

Facile synthesis of iminated lignin for enhanced free radical and lead ion scavenging capabilities

Kraft lignin (KL) holds significant potential as a renewable resource for the development of innovative materials that are currently not fully utilized. In this study, a novel iminated lignin (IL) was synthesized by grafting primary amine lignin (N−KL) onto salicylaldehyde. The effects of the dosage and reaction temperature on the nitrogen content of N-KL were evaluated. The maximum nitrogen content in N-KL reached to 3.32 %. Characterization by spectroscopy techniques (FT-IR, XPS, and NMR), elemental analysis, and gel permeation chromatography confirmed the imination of lignin. Additionally, the antioxidant activity of the lignin samples was investigated using the 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging ability. Moreover, the DPPH radical scavenging capacity of IL-6 (IC50 = 38.6 ± 3.9 μg/mL) was close to that of commercial antioxidant butylated hydroxytoluene (BHT) (IC50 = 37.7 ± 4.5 μg/mL). Furthermore, the adsorption equilibrium results indicated that IL-6 had a maximum uptake of 115.6 mg/g Pb2+, which was 3.2-fold higher than that of KL. Kinetic adsorption experiments suggested that IL-6 adsorption follows a pseudo-second-order model. Therefore, the synthesized iminated lignin is a promising candidate for the development of environmentally friendly materials with applications as an antioxidant and lead-ion adsorbent.

Hydrophobic CHA-ZIFs with a junctional trap between cha and d6r cages for adsorption of 2,3-butanediol in aqueous solution

Hydrophobic CHA-ZIFs with a junctional trap between cha and d6r cages for adsorption of 2,3-butanediol in aqueous solution

Adsorption of Cr(VI) and Cr(III) on layered pipe scales and the effects of disinfectants in drinking water distribution systems

Pipe scales in drinking water distribution systems (DWDS) potentially adsorb chromium (Cr). Meanwhile, the fate of Cr in pipe scales and water could be influenced by the disinfectants used in DWDS since they might influence the valence state of Cr. Therefore, the adsorption of Cr (Cr(VI) and Cr(III)) on pipe scales, the transformation between different valence states, and the effects of disinfectants present in DWDS are important research topics for improving tap water quality but have not yet been sufficiently investigated. This study investigated the properties of layered pipe scales and conducted adsorption kinetic experiments in single and binary Cr(VI) and Cr(III) systems, as well as experiments related to the oxidation and adsorption of Cr(III) under the influence of decaying disinfectants. According to the results, pipe scales exhibited distinct layered structures with varying mechanisms for the adsorption of Cr(VI) and Cr(III). Cr(VI) was adsorbed through surface complexation on the surface and porous core layers, while redox reactions predominantly occurred on the shell-like layer. Furthermore, Cr(III) was adsorbed via surface precipitation on the three-layer pipe scales. Importantly, disinfectants promoted the transformation of Cr(III) to the less readily released Cr(VI) in pipe scales, reducing the Cr exposure risk from the pipe scale phase. Pipe scales also decreased the Cr(VI) concentration in water (almost 0 mg/L), enhancing the safety of DWDS. This study provides theoretical guidance on the safe operation of DWDS.

High selectivity molecularly imprinted polymer based on short amylose as bio-based functional monomers for selective extraction of λ-cyhalothrin

Nowadays, the development of sustainable molecularly imprinted polymers (MIPs) with high selectivity is still challenging due to the limitations of bio-based functional monomers. In this study, the highly selective and porous MIPs (LC-TMIPs) were designed and prepared on short amylose (SAM) as bio-based functional monomers, λ-cyhalothrin (LC) as a template molecule, and tetrafluoroterephthalonitrile as a rigid crosslinking agent. Static, dynamic, and selective adsorption experiments were conducted to investigate the adsorption performance. The results indicated that, compared to MIPs prepared using epichlorohydrin as flexible crosslinking agents, LC-TMIPs exhibited higher imprinting factor (3.93), selectivity (5.78), and adsorption capacity (35.79 mg g−1), as well as faster adsorption/desorption kinetics. The LC-TMIPs were used as sorbents for the selective determination of LC in both apple and cucumber samples by high-performance liquid chromatography. Under the optimal extraction conditions, the recoveries of the method reached 92.1–106.1 %, with a linear range of 1.5–30 ng g−1 and a detection limit of 0.5 ng g−1. The proposed preparation method of LC-TMIPs is expected to open a new way to prepare highly selective and sustainable MIPs for hydrophobic compounds.

Selective adsorption and separation of salicylic acid and 4‐hydroxyisophthalic acid from industry‐grade 4‐hydroxybenzoic acid on UiO‐66

AbstractIn this study, UiO‐66 was employed for the first time as an adsorbent to separate phenolic acid analogues, specifically 4‐hydroxyisophthalic acid and salicylic acid, from impurities. Synthesized in‐house, UiO‐66 was shown to exhibit high selectivity towards 4‐HIPA/4‐HBA and SA/4‐HBA when a molar equivalent of acetic acid modulator to terephthalic acid was set at 44. The adsorption capacities for 4‐HBA, 4‐HIPA, and SA were determined to be 56.34, 55.02, and 60.34 mg/g, respectively. Furthermore, it was observed that after six regeneration cycles, the adsorption capacity for 4‐HBA remained nearly unchanged, whereas those for 4‐HIPA and SA decreased by 5.6% and 2.6%, respectively. FTIR and XPS analyses revealed that all three compounds were adsorbed at the same dominant Zr cluster site on UiO‐66, primarily through hydrogen bonding and electrostatic interaction. Dynamic adsorption experiments revealed that 4‐HBA was the first to elute, maintaining the residual contents of 4‐HIPA and SA below 0.1 wt%. Compared to traditional separation techniques, this paper provided a simple and effective method to purify industrial grade 4‐hydroxybenzoic acid.

In situ synthesis of porous metal-organic frameworks NH2-UiO-66 on tea stem biochar and application in odours adsorption

Multiple odour nuisance in livestock farming is a notorious problem that has a significant impact on the living environment of surrounding communities. Adsorbents based on metal-organic framework (MOF) materials show great promise for controlling odour pollution, as they offer a high specific surface area, a controllable structure and an abundance of active sites. However, the MOF formation process is prone to problems such as pore clogging or collapse and reduced porosity, which limits its further application. In this study, a series of odour adsorbents were prepared by in situ growth of NH2-UiO-66 on tea stem biochar (TSBC) using a hydrothermal method and named UiO (Zr)-TSBCx. The physical and chemical properties and composition of UiO (Zr)-TSBCx have been systematically characterized using SEM, TEM, XRD, FT-IR, N2 adsorption-desorption and XPS. The release of odours from the pig farm effluent was monitored using in-situ continuous Proton-Transfer-Reaction Mass Spectrometry (PTR-MS), and the obtained primary compositions were tested for further adsorption. In dynamic adsorption experiments focused on butyric acid, UiO (Zr)-TSBC2 showed a high adsorption capacity of 3.99 × 105 μg/g and exceptional structural stability. UiO (Zr)-TSBC2 showed variable adsorption efficiencies for different odorous gases, with the best performance for the removal of ammonia, toluene and butyric acid. It also demonstrated the ability to rapidly mitigate instantaneous high concentrations of hydrogen sulfide (H2S), methanethiol and toluene resulting from agitation. Additionally, based on the relationship between the adsorption amount and the structural characteristics of the adsorbent as well as the nature of the odours, a possible adsorption mechanism of UiO (Zr)-TSBC2 for a variety of odours released from pig farm effluent was proposed. This work demonstrates a novel approach to promote deodorization applications in livestock and poultry farming environments by the in-situ growth of NH2-UiO-66 on biochar prepared from tea stem.

Influence of biochar on the removal of Microcystin-LR and Saxitoxin from aqueous solutions

The present study assessed the effective use of biochar for the adsorption of two potent HAB toxins namely, Microcystin-LR (MCLR) and Saxitoxin (STX) through a combination of dosage, kinetic, equilibrium, initial pH, and competitive adsorption experiments. The adsorption results suggest that biochar has excellent capabilities for removing MCLR and STX, with STX reporting higher adsorption capacities (622.53–3507.46 µg/g). STX removal required a minimal dosage of 0.02 g/L, while MCLR removal needed 0.4 g/L for > 90%. Similarly, a shorter contact time was required for STX removal compared to MCLR for > 90% of toxin removed from water. Initial pH study revealed that for MCLR acidic conditions favored higher uptake while STX favored basic conditions. Kinetic studies revealed that the Elovich model to be most suitable for both toxins, while STX also showed suitable fittings for Pseudo-First Order and Pseudo-Second Order in individual toxin systems. Similarly, for the Elovich model the most suited kinetic model for both toxins in presence of each other. Isotherm studies confirmed the Langmuir–Freundlich model as the best fit for both toxins. These results suggest adsorption mechanisms including pore filling, hydrogen bonding, π–π interactions, hydrophobic interactions, electrostatic attraction, and dispersive interactions.

Arsenic and fluoride adsorption from multielement solutions onto aluminium modified montmorillonite

Groundwater is the primary source of drinking water worldwide. However, it might be harmful to consumer's health due to the presence of trace elements, such as arsenic and fluoride, commonly found in Latin American. The main objective of this study was to investigate the adsorption parameters of arsenic (As) and fluoride (F) dissolved in multielemental solutions containing vanadium (V) and boron (B), on aluminium-modified montmorillonite. To achieve that, a new adsorbent was synthesised and characterised using X-ray diffraction spectroscopy (XRD), Scanning Electron Microscopy (SEM) coupled with Energy Dispersive X-Ray (EDX) and N2 adsorption/desorption isotherm techniques. Adsorption efficiencies for As and F were evaluated in multielement solutions considering the simultaneous occurrence of B and V, naturally present in groundwater. Kinetic and equilibrium adsorption experiments were carried out in batch conditions for both, mono and multicomponent solutions. The adsorbent characterization indicated an effective incorporation of Aluminium (Al) into the aluminosilicate layers and at the external surface of the montmorillonite. The adsorption process for multielement solutions took a short time and the As adsorption was not affected by the presence of V, B, or F in the solution while F adsorption parameters were enhanced by the co-occurrence of the other species in the solution. The maximum adsorption capacities were 21 and 68 mg g−1 for As and F, respectively, in the presence of B and V, at low adsorbent dosage. The new material was also tested for groundwater samples collected from Buenos Aires province (Argentina) that were naturally contaminated with As, V, B, and F. The removal of these elements was lower when compared to synthetic solutions. However, the material's efficiency in removing the ions from natural groundwater was approximately 50%. These results suggest that the material could be used to develop filters to remediate arsenic and fluoride from naturally contaminated groundwater.

Performance on adsorption of toluene by ionic liquid-modified AC in high-humidity exhaust gas.

Volatile organic compounds (VOCs) frequently pose a threat to the biosphere, impacting ecosystems, flora, fauna, and the surrounding environment. Industrial emissions of VOCs often include the presence of water vapor, which, in turn, diminishes the adsorption capacity and efficacy of adsorbents. This occurs due to the competitive adsorption of water vapor, which competes with target pollutants for adsorption sites on the adsorbent material. In this study, hydrophobic activated carbons (BMIMPF6-AC (L), BMIMPF6-AC (g), and BMIMPF6-AC-H) were successfully prepared using 1-butyl-3-methylimidazolium hexafluorophosphate (BMIMPF6) to adsorb toluene under humidity environment. The adsorption performance and mechanism of the resulting ionic liquid-modified activated carbon for toluene in a high-humidity environment were evaluated to explore the potential application of ionic liquids as hydrophobic modifiers. The results indicated that BMIMPF6-AC-H exhibited superior hydrophobicity. The toluene adsorption capacity of BMIMPF6-AC-H was 1.53 times higher than that of original activated carbon, while the adsorption capacity for water vapor was only 37.30% of it at 27 °C and 77% RH. The Y-N model well-fitted the dynamic adsorption experiments. To elucidate the microscopic mechanism of hydrophobic modification, the Independent Gradient Model (IGM) method was employed to characterize the intermolecular interactions between BMIMPF6 and toluene. Overall, this study introduces a new modifier for hydrophobic modification of activated carbon, which could enhance the efficiency of activated carbon in treating industrial VOCs.

An investigation into the effect of UV irradiation and biofilm colonization on adsorption and desorption behavior of polyurethane (PU) microplastics for bisphenol A (BPA)

Recent studies have demonstrated that microplastics (MPs) can act as a transport vector for pollutants in the environment. However, most studies have focused on carbon-carbon backbone polymers, with little known about heteroatom backbone polymers. In this study, polyurethane (PU) MPs were modified by UV irradiation and microorganism colonization to assess the different aging treatments on the interaction behavior (adsorption/desorption) between PU MPs and bisphenol A (BPA). The results of the adsorption kinetics experiment illustrated that the adsorption process of BPA could be described well by a pseudo-second order kinetic equation on both fresh and aged PU MPs. Although fresh PU MPs revealed the highest saturated adsorption capacity, at low BPA exposure concentrations (≤ 100 μg/L) the adsorption capacities for UV aged and biofilm colonized PU MPs were very similar to fresh MPs or even slightly higher than for fresh MPs, the main adsorption mechanisms including H-bonding interactions and π–π interactions. Fourier-transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) investigations suggested obvious physicochemical property changes (e.g., generation of new functional groups, erosion, etc.) after UV irradiation and biofilm colonization. This study also showed that different exposure environments (ultrapure water, artificial seawater, simulated gastric fluid) could affect BPA adsorption/desorption via hydrophobic and electrostatic interaction on PU surfaces. These results further clarify the adsorption mechanisms of BPA on PU MPs that have undergone different aging treatments, and provides a theoretical basis for the assessment of environmental behavior and exposure risks when PU MPs and BPA coexist.