Adsorption Of Organic Matter Research Articles

Deciphering the Roles of Molecular Weight and Carboxyl Richness of Organic Matter on Their Adsorption onto Ferrihydrite Nanoparticles and the Resulting Aggregation.

The aggregation behavior of ferrihydrite nanoparticles (FNPs) can control the fate of associated aqueous contaminants, trace elements, and organic compounds. However, FNP aggregation is difficult to predict in the presence of organic matter (OM), given the heterogeneity in the OM properties. Five model OMs based on (poly)acrylic acid (PAA or AA) and polyethylene glycol with or without terminal carboxyl groups (PEG or PEGbis, respectively) were chosen to probe the influence of key OM properties─specifically, carboxyl richness and molecular weight (MW)─and the dominant mechanisms by which they influence OM adsorption onto FNPs and the resulting aggregation. For OMs with similar MWs, those with a higher carboxyl richness adsorbed more extensively onto FNPs: PAA2k > PEGbis > PEG. Meanwhile, for OMs with the same carboxyl richness, higher MW OMs adsorbed more: PAA25k > PAA2k > AA. Furthermore, the subsequent aggregation of FNPs was largely controlled by the adsorbed mass. OMs with negligible adsorption (i.e., PEG and AA) did not change the aggregation behavior of FNPs. For OMs with low carboxyl richness (PEGbis), accelerated aggregation occurred through a bridging effect with low adsorbed mass. For OMs with high carboxyl richness (PAA2k and PAA25k), aggregation was accelerated at moderate adsorbed OM masses by patch-charge attraction and was inhibited with high adsorbed OM mass due to steric repulsion. This study provided new insights into understanding and predicting the transport and fate of FNPs and natural organic matter (NOM) in natural environments with various NOM compositions.

Hierarchically-porous resin for the adsorption of organic matter in raffinate produced by solvent extraction from the vanadium industry

Solvent extraction wastewater contains high concentrations of organic pollutants and metal ions, making it difficult to treat. This paper presents a method of using hierarchically-porous adsorption resin to recover organics from raffinate and regenerate the resin, addressing secondary pollution in extraction processes. The chosen resin, WS6108, removes over 95 % of organics from raffinate, with high metal ion concentrations enhancing its adsorption efficiency. The article conducted an optimization experiment and mechanism study on WS6108 resin for adsorbing organic matter in vanadium raffinate (OIVR), followed by desorption and recycling tests. Results showed WS6108 resin achieved a 96.7 % adsorption efficiency at a solid–liquid ratio of 24 g/L after optimization. The chosen methanol desorbent achieves over 99 % desorption efficiency for the WS6108 cycle under specific conditions. The resin’s performance remains stable for up to 45 cycles. Adsorption isotherms and kinetic experiments indicate that OIVR adsorption by WS6108 resin is endothermic, non-spontaneous and entropy increasing. Moreover, the adsorption kinetics of OIVR by WS6108 resin followed a pseudo-second-order model, based on the activation energy, liquid film diffusion was considered the main rate-controlling step. A column experiment was conducted to verify that WS6108 resin can be used in real vanadium raffinate to remove organics. Density functional theory (DFT) revealed that strong hydrogen bonding, π-π stacking and excellent adsorption diffusion behavior drive OIVR adsorption. This study aims to increase the use of adsorption to treat oily wastewater generated by solvent extraction.

Competition & UV254 projection in odorants vs natural organic matter adsorption onto activated carbon surfaces: Is the chemistry right?

Powdered activated carbon (PAC) adsorption remains an indispensable method for addressing odor problems in drinking water. While natural organic matter (NOM) is ubiquitous and competes strongly in deteriorating odorant adsorption capacity, it can also serve as a promising indicator for predicting odorant adsorption through online measurement. However, the impact of PAC surface chemistry on NOM competition and feasibility of prediction across various adsorbents are not well understood. Here, we examined the role of PAC properties (pore structure and surface chemistry) in the competitive adsorption between odorants and NOM components, aligned with the applicability assessment of using NOM optical properties for odorant adsorption projection across various PAC samples. Chemical oxidation and thermal treatment achieved considerable changes in surface functional group composition, alongside minimal changes in pore structure, of two typical PAC products with microporous/mesoporous pore characteristics. The effect of NOM interference on the reduction of odorant adsorption exhibited a similar level regardless of the PACs with different pore structure (average pore size of 1.7 nm vs. 4.2 nm). Surface modification increased the equilibrium adsorption capacity (qe50) of odorants by 15.1% to 146.4% (thermal treatment) or decreased by -81.3% to -34.1% (chemical oxidation), respectively, but minimal changes in odorant-NOM selectivity. For various odorants, hydrophobicity (log D) influenced the adsorption capacity while the structural flexibility (reflected by the rotatable bonds) affected the vulnerability of odorant adsorption to NOM competition. It was found for the first time that four-parameter Richards model (RMSE = 2.6%) is superior to the linear model (RMSE = 12.5%) or logarithmic model (RMSE = 77.6%) to describe the S-shape UV254 projection curves associated with odorant adsorption on PAC. Moreover, the feasibility was confirmed to use UV254 projection curves of pristine PAC fitted with the Richard model to predict the odorant adsorption on surface-modified PAC in two different surface waters (RMSE 9.2% and 7.4%, respectively). This study provides insight into the role of PAC surface chemistry and pore characteristics in odorant adsorption in NOM-containing waters and enhances the feasibility of the NOM surrogate model for odorant monitor and control during PAC adsorption.

Practical implications of adding powdered activated carbon in advanced wastewater treatment for process and plant design

ABSTRACT The addition of powdered activated carbon (PAC) in advanced wastewater treatment is increasingly recognized for its effectiveness in removing micropollutants from secondary effluents. This study investigates the implications of PAC dosing on treatment performance, particularly in terms of natural and effluent organic matter (OM) removal, turbidity reduction, and sludge characteristics. Results indicate that while PAC incorporation significantly enhances the adsorption of OM, it necessitates higher coagulant dosages to achieve comparable or improved turbidity levels. The study also reveals that lower pH levels facilitate the removal of OM, thereby increasing the availability of adsorption sites on PAC for micropollutants. Moreover, PAC addition results in the formation of larger, denser flocs that settle faster, leading to a reduction in sludge volume by approximately 20%. However, the increased coagulant demand and the subsequent rise in sludge volume highlight the need for the optimized process design to balance treatment efficiency with operational costs. This research provides valuable insights for the design and operation of wastewater treatment plants, emphasizing the importance of tailored coagulant dosing and process adjustments when integrating PAC into existing treatment frameworks.

Distribution characteristics of TiO2 NPs in Daihai lake and their stability regulated by abiotic factors

Accurate detection and stability analysis of titanium dioxide (TiO2 NPs) in surface water are critical for ecological risk assessment. Quantitative analysis of TiO2 NPs in water and sediment of Daihai Lake was performed and their occurrence forms was characterized by TEM, XRD and FTIR. Further investigation into the impact of pH, ionic strength (IS) and dissolved organic matter (DOM) on the stability of TiO2 NPs was carried out, along with a correlation analysis between abiotic factors and TiO2 NPs concentration. Results showed that TiO2 NPs in water and sediment are 1.01 × 105 and 5.66 × 105 particles/mL in July 2023, respectively. After transformed in water sample from Daihai Lake, the hydrodynamic particle (HDD) of TiO2 NPs reach 600–700 nm, with reduced crystallinity and observable characteristic peaks of NaCl, which is related to the high concentration of NaCl in Daihai Lake. Structural defects and changes in surface properties of TiO2 NPs are introduced due to the adsorption of organic matter, leading to higher aggregation and sedimentation rates. Specifically, Ca2+ promote the sedimentation of TiO2 NPs more than Na+. Conversely, A/A0 increased to 0.80–0.94 from 0.64 after humic acid (HA) and fulvic acid (FA) added. Hydroxyl and carboxyl groups of FA enhanced steric hindrance and inhibited TiO2 NPs sedimentation. While a strong promotion effect on the sedimentation of TiO2 NPs is detected when 10 mmol/L Ca2+ coexisted with 10 mg/L HA, with 70% of the TiO2 NPs settled within 120 min. Additionally, the concentration of TiO2 NPs in Daihai Lake is significantly positively correlated with dissolved organic carbon (DOC) and humification index, which might be relate to the enhancement of TiO2 NPs stability of aromatic organic matter. And the high concentration of DOC will also lead to the stable existence of TiO2 NPs in water and exacerbate aquatic toxicity.

Enrichment Mechanism of Polymetallic Elements at the Base of the Niutitang Formation in Southeast Chongqing

Polymetallic enrichment layers are commonly found at the base of the Lower Cambrian and extensively distributed across the Upper Yangtze Platform, yet their genetic models remain controversial. This study systematically collected samples from a typical section in the southeastern Chongqing region for mineral, organic, and inorganic analyses. It investigates the relationship between the abundance of various trace metal elements and organic matter at the base of the Niutitang Formation, as well as the vertical distribution characteristics of organic carbon isotopes and organic matter features. The results indicate that the Niutitang Formation shale exhibits a distinct three-part structure from bottom to top. Various metal elements are enriched in the lower interval, showing a close correlation between the abundance of polymetallic elements and the carbon isotopes of shale organic matter. The middle interval contains the highest TOC value and the lowest Ti/Al ratio, while the upper interval shows a significant decrease in organic matter abundance, with a clear positive correlation between the excess silicon content and Ti/Al ratio. Additionally, the mixing effect of deep-sea upwelling is the primary control on the formation of polymetallic enrichment layers in the lower interval, followed by the adsorption of organic matter under anoxic conditions. The sedimentary environment of the upper interval of the Niutitang Formation trends toward oxidation, with paleoclimate shifting toward colder and drier conditions, exhibiting aeolian sedimentary features that are unfavorable for the enrichment of trace metal elements. Consequently, upwelling is a key factor in the enrichment and mineralization of trace metal elements at the base of the Lower Cambrian in the Upper Yangtze region.

Recent advances in MXene nanomaterials: Fundamentals to applications in environment sector

AbstractMXenes are a new type of 2D transition metal carbon/nitride or carbonitride, which are composed of Mn+1AXn phase material (MAX phase) through single‐layer or thin‐layer nanosheets obtained by exfoliation. Owning to unique two‐dimensional layered structure, large specific surface area, excellent electrical conductivity and mechanical stability, the MXenes have quickly become a research hotspot due to their magnetic and other properties, and have been widely used in many fields such as electrochemical sensors, energy storage, catalysis, and adsorption. This article summarizes and introduces preparation methods of two‐dimensional materials MXenes, and focus on reviewing their application research progress in the electrochemical sensors and environmental field in recent years, including detection of biomarkers and environmental pollutants, adsorption of heavy metals, adsorption of radiation metals, adsorption of organic matter, selective adsorption of carbon dioxide, membrane separation, sensors, electrocatalysis, photocatalysis, electromagnetic absorption and shielding, etc. A summary and review were conducted, and finally the existing problems and future development at this stage were analyzed.

Studying the Effect of Chemical Activated Kaolinite on Organic Matter Adsorption from Crude Phosphoric Acid (H3PO4)

Studying the Effect of Chemical Activated Kaolinite on Organic Matter Adsorption from Crude Phosphoric Acid (H3PO4)

Effects and Mechanisms of Different Types of Biochar on Heavy Metal Passivation during Sludge Composting.

The effects and mechanisms of the different types of biochar on heavy metal passivation are still not fully understood. This study compared the effects of three types of biochar on heavy metal passivation during sludge composting. Compared with composting without biochar, rice husk biochar was most effective for the passivation of Zn and Pb, with increased passivation rates of 1.90% and 20.43%, respectively. In contrast, sludge biochar was the most effective for the passivation of Cr and Hg, with increased passivation rates of 28.30% and 3.09%, respectively. Coconut shell biochar showed the best performance for the passivation of Cu, Ni, As, and Cd, and was enriched with micropore structures, which possibly led to the adsorption and reaction of heavy metals, organic matter, and microorganisms. The improved passivation effect of the rice husk and sludge biochar on heavy metals can be attributed to the improved humification of organic matter. This study suggests that specific types of biochar should be considered for the passivation of different types of heavy metals for practical applications.

Nitrogen fertilisation reduces the contribution of root-derived carbon to mineral-associated organic matter formation at low and high defoliation frequencies in a grassland soil

Abstract Background and aims Rhizodeposition is organic matter released by living plant roots that can be transformed by microbes into particulate organic matter (POM), but that can also become more stable through the adsorption of organic matter onto soil minerals (mineral-associated organic matter, MAOM), thereby playing an important role in mitigating climate change. We examined how root-derived carbon (C) as a proxy for rhizodeposition contributed to POM and MAOM formation in a grassland affected by nitrogen (N) fertilisation and defoliation frequency, and to what degree rhizodeposition was incorporated into microbial biomass. Methods We applied N fertiliser (0 vs. 40 kg N ha−1 yr−1) and defoliation frequencies (3–4 vs. 6–8 clipping events year−1, simulating low and high grazing intensity) for three years, then used a 13CO2 pulse labelling technique to examine the incorporation of rhizodeposition into microbial biomass, POM and MAOM fractions. Results With N fertilisation, rhizodeposition contributed less to the formation of MAOM compared to the formation of POM, while defoliation frequency decreased the contribution of rhizodeposition into both POM and MAOM, particularly with N fertilisation. Although the MAOM fraction was relatively rich in N (C: N ratio of 10.5 vs. 13.5 for POM), our results suggest that adding inorganic N promoted the formation of POM more than of MAOM from rhizodeposition. Conclusion A large proportion of rhizodeposition was taken up by microbes that eventually could contribute to POM and MAOM formation. Our results provide insightful information regarding the stabilisation of rhizodeposition into different soil organic matter pools.

Investigating the use of CaCO3 particles synthesized in the Ca(OH)2-CO2-H2O system for organic matter removal: adsorption efficiency and recyclability

ABSTRACT In this study, we experimentally investigate the production and characterization of CaCO3 particles through the carbonation process of Ca(OH)2 and evaluate their potential application in removing organic matter. The CaCO3 particles were characterized using BET, SEM-EDX, FT-IR, particle size, and XRD techniques. Adsorption of organic matter was studied using synthetic solutions and samples from two surface water sources. Experiments were conducted at room temperature with adsorbent dosages ranging from 1.3 to 21.5 g/L, initial dissolved organic carbon concentrations between 2.5 and 20 mg/L (initial loading: 0.1–14.6 mgDOC/gCaCO3), and a contact time of at least 5 minutes. We observed a removal efficiency of 70–80% for DOC and 90–95% for UV254 at a low concentration of organic matter (humic acids, 2.5 mgDOC/L). At a concentration of 5.0 mg DOC/L, we achieved (i) 70–90% DOC removal for humic acid, (ii) 50–65% DOC removal for one surface water sample with SUVA254 of 2.4 L/mg·m, and (iii) 20–35% DOC removal for another surface water sample with SUVA254 of 4.3 L/mg·m. Furthermore, we investigated the performance of the prepared particles in repeated usage for organics removal. In conclusion, our findings propose areas for future research including optimizing particle cycling within the reaction environment, exploring particle utilization in reactors such as an up-flow particle bed, and assessing potential applications in a membrane contactor. The environmentally friendly and non-toxic nature of CaCO3 particles emphasizes their significance in future research and applications.

Compositional differences of near-critical petroleum from closed pores to wellhead in Gulong shale oil play, Songliao Basin, NE China

The Gulong shale oil play located in northern Songliao Basin is a promising exploration target in China. Member 1 of Qingshankou Formation (Well H) with high thermal maturity was preferred to obtain pressure-retained cores, long-time exposed cores, and produced petroleum (crude oil and gas). The selected samples were subjected to sequential extraction, GC, GC-MS, thermal desorption–gas chromatography (TD-GC) and Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) analysis. The compositional differences of in-situ fluids, residual bitumen trapped in open, confined, and closed pores, as well as wellstream, were systematically investigated. (1) In-situ fluid compositions, with a 30.8% proportion of nC1−5 in n-alkanes, were studied by TD-GC analysis on pressure-retained cores. Interestingly, limited amounts of C8- compounds were detected in long-time exposed bulk cores but were almost absent in exposed powder. Primally poor pore connectivity and partially adsorption or absorption of organic matter contribute to the retention of gaseous hydrocarbons. (2) Sequential extraction is a best method for obtaining compositions of fluid in pores with variable sizes. Aliphatic compounds of residual bitumen trapped in open pores are similar to those in confined pores, while polar compounds are more enriched in confined and closed pores. Originally connected pores in early oil window, has turned into confined or closed pores by compaction and cementation with increasing depth. (3) Wellstream compositions are significantly different from in-situ fluid compositions, especially in shale oil extraction. The proportion of gaseous hydrocarbons in the wellstream (76.2%) is considerably higher than that of in-situ fluids (34.1%). Comparison of aromatic hydrocarbons indicated that the wellstream is sourced from free fluids and partially adsorbed hydrocarbons in open pores. (4) Nitrogen and oxide compounds with a higher degree of condensation (higher DBE value) have poor movability, leading to extremely low content or even absence in crude oil. The compositional differences from in-situ fluids to the wellbore through the stimulated fractures are caused by selective adsorption of pore walls, confinement effect of nanopores and fluid phase changing. This study provides a window to the compositional differences of fluids released from different occurrence spaces and confirms compounds heterogeneity.

Simultaneous Cd2+ and organic matter sorption behavior on various microplastics: Modeling of influencing factors using the Taguchi method

In aquatic environments, microplastics (MPs) can serve as a vector for pollutants. Pollutants adsorbed on the surface of microplastics pose a potential risk to aquatic organisms. In this study, the effect of environmental conditions such as duration, pH and conductivity on the Cd+2 and organic matter adsorption capacity, qe,Cd and qe,COD of microplastic type was evaluated using the Taguchi experimental design method. ANOVA results showed that the most effective factor in adsorption capacity was the microplastic type. qe,Cd were listed as > 0.6–0.8 mg/gPP, >0.4 mg/gMDPE, 0.2 mg/gLDPE at 50 mS/cm. It was observed that conductivity had a positive effect on qe,Cd.,qe,Cd for PP in waters with conductivities of 50 mS/cm, 0.8 mS/cm, 0.02 mS/cm at pH 7.0 was found to be ≫ 0.6, >0.2, > 0.4, respectively. qe,Cd and qe,COD showed similar trends. It was determined that the qe,COD at 50 mS/cm was in the order of 15–22 mg COD/gPP, 5–10 mg COD/gMDPE, but not determined for LDPE. After MW and UV artificial aging, qe,COD of virgin PP increased by 31.5 % and 94.4 %, respectively, whereas the qe,Cd decreased by 1.2 % and 24 %.

Salinity influence on adsorption of lipid molecules in clay minerals: Results from experiments and calculations

Model compounds, such as 12-Aminohexadecanoic acid and kaolinite, mare utilized to simulate adsorption under different salinities. The experiments showed that the total organic carbon content adsorbed to kaolinite is 0.166% and 0.082% under high and low salinity conditions, respectively. The kaolinite (001) adsorption behavior of organic matter was simulated by molecular dynamics (MD) technology in the presence of Na+. In addition, the adsorption process was not only statistically analysed but the adsorption energy of state organic matter at the clay surface and the sources of adsorption energy are calculated. It is shown that the increase of Na+ is conducive to the adsorption of the organic matter, which is also supported by the experimental results. The adsorption of organic matter is mainly controlled by functional groups of -CH2 on the kaolinite surface. Density functional theory (DFT) calculations further indicate that the 2 s orbital of Na+ is hybridized with -OH of kaolinite and the 2p orbital of -COO- of 12-Aminohexadecanoic acid under bridging action. Thus, the electron compensation mechanism of Na+ was clarified. This study provides a molecular perspective on the interaction mechanisms between organic matter and kaolinite, which is beneficial to the field of biogeochemistry and environmental effects.

Contrasting mixed scaling patterns and mechanisms of nanofiltration and membrane distillation

Oriented towards the pressing needs for hypersaline wastewater desalination and zero liquid discharge (ZLD), the contrasting mixed scaling of thermal-driven vacuum membrane distillation (VMD) and pressure-driven nanofiltration (NF) were investigated in this work. Bulk crystallization was the main mechanism in VMD due to the high salinity and temperature, but the time-independent resistance by the adsorption of silicate and organic matter dominated the initial scaling process. Surface crystallization and the consequent pore-blocking were the main scaling mechanisms in NF, with the high permeate drag force, hydraulic pressure, and cross-flow rate resulting in the dense scaling layer mainly composed of magnesium-silica hydrate (MSH). Silicate enhanced NF scaling with a 75% higher initial flux decline rate attributed to the MSH formation and compression, but delayed bulk crystallization in VMD. Organic matter presented an anti-scaling effect by delaying bulk crystallization in both VMD and NF, but specifically promoted CaCO3 scaling in NF. Furthermore, the incipient scaling was intensified as silicate and organic matter coexisted. The scaling mechanism shifted from surface to bulk crystallization due to the membrane concentration in both VMD and NF. This work fills the research gaps on mixed scaling mechanisms in different membrane processes, which offers insights for scaling mitigation and thereby supports the application of ZLD.

Interaction of microorganisms with carbonates from the micro to the macro scales during sedimentation: Insights into the early stage of biodegradation

The assembly process of Organic Matter (OM) from single molecules to polymers and the formation process of Ca–CO3 ion-pairs are explored at the micro-scale, and then the relationship between OM and carbonate based on the results of microbially-induced carbonate precipitation (MICP) laboratory experiments is established at the macro-scale. Molecular dynamics (MD) is used to model the assembly of OM (a) in an aqueous solution, (b) on surfaces of calcite (10 1‾ 4) crystals and (c) on defective calcite (101‾ 4) crystal surfaces. From the MICP experiments, carbonate minerals containing abundant OM were precipitated and were characterized by Scanning Electron Microscopy (SEM), X-Ray Diffractometry (XRD) and Fourier Transform Infrared Spectroscopy (FTIR). The results of the MD show that OM is assembled into polymers in all three simulation systems. Although the Ca–CO3 ion-pairs and OM were briefly combined, the aggregation assembly of OM molecules and the precipitation of carbonate calcium are not related in the long run. The highly specific surface area of the defective calcite shows an increase in the adsorption of OM. The van der Waals forces, which are primarily responsible for controlling the assembly of OM molecules, increase with the degree of aggregation. According to the MICP experiments, OM is enriched on the mineral surfaces, and more OM is found at the steps of defective crystals with their larger surface areas. Through MD and MICP laboratory experiments, this work systematically describes the interaction of OM and carbonate minerals from the micro to the macro scales, and this provides insight into the interaction between OM and carbonates and biogeochemical processes related to the accumulation of OM in sediments.

Selective Hydrogenolysis of Furfuryl Alcohol to Pentanediol over Pt Supported on MgO

The catalytic conversion of naturally rich and renewable biomass into high-value chemicals is of great significance for pursuing a sustainable future and a green economy. The preparation of pentanediol from furfuryl alcohol is an important means of high-value conversion of biomass. The Pt-based catalyst supported on MgO was applied to the selective hydrogenation of biomass furfuryl alcohol to prepare pentanediol. By adjusting parameters such as catalyst loading, reduction temperature, reaction temperature, and pressure, a highly active catalyst was designed and the optimal catalytic hydrogenation conditions were determined. The hydrogenation experiment results showed that the selectivity of the 2Pt/MgO-200 catalyst for 1,2-pentanediol and 1,5-pentanediol reached 59.4% and 15.2%, respectively, under 160 °C and 1 MPa hydrogen pressure. The catalyst was characterized by X-ray powder diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectrometer (XPS), CO2-temperature programmed desorption (CO2-TPD), and other methods. The characterization results indicate that the reduction temperature has a significant impact on the metal Pt, and an appropriate reduction temperature is beneficial for the hydrogenation performance of the catalyst. In addition, the basic sites on the carrier are also another important factor affecting the activity of the catalyst. In addition, stability tests were conducted on the catalyst, and the reasons for catalyst deactivation were studied using methods such as thermogravimetric analysis (TGA) and Fourier transform infrared spectroscopy (FT-IR). The results showed that the activity of the catalyst decreased after five cycles, and the deactivation was due to the hydrolysis of the carrier, the increase in metal particle size, and the surface adsorption of organic matter.

Growth of TiO2/Ti-MOF nanorod array with enhanced photoabsorption and photocatalytic properties on carbon cloth for efficient auto-cleaning solar desalination

Solar-enabled seawater desalination has attracted increasing attention for mitigating the freshwater crisis worldwide, while the practical applications are vitally restricted due to unsatisfactory photoabsorption and membrane contaminations from organic-matter adsorption and sea-salt deposition. To settle the above issues, herein we report the growth of TiO2/NH2-MIL-125(Ti) nanorod array with enhanced photoabsorption and photocatalytic properties on carbon fiber cloth (CFc) (abbreviated as CFc/TiO2/Ti-MOF) by a simple hydrothermal-solvothermal two-step process for efficient auto-cleaning solar desalination. CFc/TiO2/Ti-MOF exhibits super-hydrophilicity (contact angle of 0° at 5 s) and higher photoabsorption (89.5 %) due to the surface modification and light-trapping effect from TiO2/Ti-MOF nanorod array, compared with CFc substrate (contact angle of 118° at 8 s, photoabsorption of 86.3 %). When CFc/TiO2/Ti-MOF is immersed in the aqueous solution containing organic dyes as pollutant model, it can remove 76.4 % Rhodamine B (RhB), 94.1 % methylene blue (MB), 62.8 % tetracycline (TC) and 58.5 % ofloxacin (OFLX) in 120 min under one sun irradiation. Subsequently, such CFc/TiO2/Ti-MOF cloth is used to construct a hanging evaporator, and it exhibits high evaporation rate of 1.86 kg m−2 h−1 without the solid-salt precipitation, conferring long-term auto-cleaning evaporation. Therefore, this study provides some insights for designing novel photothermal/photocatalytic membranes for efficient auto-cleaning solar desalination.

Interfacial quantum chemical characterization of aromatic organic matter adsorption on oxidized microplastic surfaces

Examining the adsorption efficiency of individual contaminants on microplastics (MPs) is resource-intensive and time-consuming. To address this challenge, combined laboratory adsorption experiments with model simulations were performed to investigate the adsorption capacities and mechanisms of MPs before and after aging. Our adsorption experiments revealed that aged polyethylene (PE) and polyvinyl chloride (PVC) MPs exhibited increased adsorption capacity for benzene, phenol, and naphthalene. Additionally, density functional theory (DFT) simulations provided insights into changes in adsorption sites, adsorption energy, and charge density on MPs. The π bond of the benzene ring emerged as a pivotal factor in the adsorption process, with van der Waals forces exerting dominant influence. For instance, the adsorption energy of benzene on pristine PE was −0.01879 eV. When oxidized groups, such as hydroxyl, carbonyl, and carboxyl, on the surface of aged PE became the adsorption sites, the adsorption energy increased to −0.06976, −0.04781, and −0.04903 eV, respectively. Regions with unoxidized functional groups also exhibited higher adsorption energies than pristine PE. These results indicated that aged PE had a stronger affinity for benzene compared to pristine PE, enhancing its adsorption. Charge density difference and energy density of states corroborated this observation, revealing larger π-bond charge accumulation areas for benzene on aged PE, suggesting stronger dipole interactions and enhanced adsorption. Similar trends were observed for phenol and naphthalene. In summary, the DFT calculations aligned with the adsorption experiment findings, confirming the effectiveness of simulation methods in predicting changes in the adsorption performance of aged MPs.

Fractionation of stable boron isotopes in alfisols: Application of a novel tool for tracing boron behavior in two soil profiles

Available boron (AB) and total boron (TB) in soil have distinct isotopic values, which are mainly influenced by the pH, organic matter and clay minerals, and can be used to explore the chemical behaviors of boron (B) in adsorption, weathering and eluviation processes. The B isotopic compositions of AB and TB in brown soil (slightly acidic) and cinnamon soil (neutral to slightly alkaline) profiles were investigated by multicollector inductively coupled plasma mass spectrometry. Variations in pH value and organic matter in the two soils directly affected the adsorption of B isotopes (dissolved 11B(OH)3 or 10B(OH)4-) in the aqueous solution, as shown by AB having an average negative δ11B value of −1‰ and a great range of −10.83‰ to +8.32‰ in the cinnamon soil. Furthermore, the long-term effects of adsorption and transportation processes were evidenced by the large range of δ11BTB values (-24.22‰ to +21.07‰) in the two soils. The topsoil layers with more organic matter and higher δ11B values indicated that B isotope fractionation occurred as a result of the input of rainfall, recycling of plant litter and the adsorption of organic matter and clay minerals. The lower δ11B values, the higher B contents and the element ratios in the underlying layers resulted from the weathering of different minerals and the adsorption of AB in the leaching process. This finding is supported by the relationship between AB and the clay/silt ratio, with more negative δ11B values being associated with finer clay particles via the adsorption of 10B(OH)4- in a weakly alkaline soil solution. The δ11B values in soils may be a useful tool for distinguishing geochemical cycling and processes and characterizing long-term processes that are difficult to assess.