Adsorption-desorption Behavior Research Articles

Adsorption-desorption behavior of malachite green on aged microplastics in seawater environment

The role of microplastics (MPs) as carriers of contaminants in the water environment is an emerging concern, significantly impacting migration and transformation. This study aims to compare the adsorption behavior of MPs with Malachite green (MG) dye before and after simulated short-term seawater aging (especially during the initial phase of the aging process) and to analyze in-depth the mechanism by which the aging process influences adsorption behavior. Results showed that after aging, the adsorption capacities of Polypropylene (PP), Polyethylene terephthalate (PET), and Polyethylene (PE) for MG were 2.58, 2.43, and 1.59 mg g−1, respectively. The adsorption capacity of other MPs for MG increased significantly, except for PE, which remained nearly unchanged. Calcium chloride (CaCl2) plays a significant role in the seawater aging process, and increasing the concentration of CaCl2 leads to a decrease in the adsorption amount of MG. Additionally, the adsorption capacity for MG varies significantly across different particle sizes and types of MPs, as well as the adsorption capacity of PP for different dyes. The Langmuir and Freundlich models indicate that the adsorption aligns more with the Freundlich model, which suggests that adsorption primarily occurs as multi-layer adsorption on a non-homogeneous surface. These results provide a scientific foundation for evaluating the ecological and environmental risks when MPs and organic dyes coexist. We also propose a novel approach of “treating waste dye with MPs” to mitigate their pollution in the aquatic environment.

Strychnos potatorum seeds derived magnetic graphene oxide nanocomposite for removal of nickel from wastewater: Adsorption performance, isotherm, kinetic and desorption behavior

In the present study investigates the adsorption of nickel ions by Strychnos potatorum seeds derived magnetic graphene oxide (SP-MGO). The fitness of the derived material was analyzed using BET and zeta seizer which proves the suitability of this adsorbent for adsorption process. The surface area, pore size and pore volume were obtained through BET analysis and the results were 51.798 (m2/g), 16.795 nm and 0.217 (cm3/g) respectively. And the size of the nanoparticle was measured using zeta seizer. For achieving maximum adsorption capacity, the following optimized conditions were; 60 min of contact time, under pH of 8, with 10 mg of SP-MGO dose, for the concentration of 10 mg/l, at the temperature of 35 °C. Freundlich isotherm (R2 =0.999) and pseudo second order (R2 =0.997) was well described the adsorption process. According to the isotherm model the adsorption of nickel ions occurs by multilayer of adsorption on heterogeneous surface of SP-MGO nanoadsorbent and also by chemisorption according to kinetic model. The Langmuir monolayer adsorption capacity (Q max) obtained by SP-MGO was 6.66 mg/g. The regeneration ability of SP-MGO was only reduced 17.1 % even after five cycles of adsorption runs. Overall, the SP-MGO can be a potential option for develop into a commercial adsorbent for industrial use to eliminate the pollutants from waste water.

The adsorption–desorption behavior of 2,4-dichlorophenol on microplastics in waters with different salinity

The adsorption–desorption behavior of 2,4-dichlorophenol on microplastics in waters with different salinity

Asymmetrical anchor way of manganese atoms on carbon domain edge for enhanced oxygen reduction reaction

Single atomic catalysts (SACs), especially the catalysts featured by well-developed M-N4 moieties, show excellent catalytic activity and spark enormous attention. However, the highly symmetric active sites may result in some degenerate electronic states for the d orbitals of the center metal atom, which suffer from the unsatisfactory adsorption-desorption behaviors during reaction. Herein, we develop an asymmetric anchor site by two types of nitrogen (sp-N and pyridinic N) created in the inherent edge-rich carbon domain of hydrogen-substituted graphdiyne (HsGDY), where atomic catalyst like manganese atoms can be asymmetrically anchored on the one side of hexagon carbon rings. The abundant elegant hexagon carbon rings on HsGDY not only facilitate the creation of edge sites, but also provide available space for the coordination of terminal ligands (OH) with Mn atoms. The as-synthesized Mn-N-HsGDY exhibits excellent ORR activity and an impressive long-term cyclability for over 3800 cycles in a rechargeable Zn-air battery.

The adsorption-desorption behavior of chlorothalonil in the cuticles of apple and red jujube

The distribution fate of chlorothalonil (CHT) in the environment (soil and water) and fruits is controlled by the capacity of cuticles to adsorb and desorb CHT, which directly affects the safety of both the environment and fruits. Batch experiments were conducted to reveal the adsorption-desorption behaviors of CHT in the cuticles of apple and red jujube. The adsorption kinetics showed that both physisorption and chemisorption occurred during the adsorption process. Furthermore, the isothermal adsorption of CHT in the fruit cuticles followed the Freundlich model. The thermodynamic parameters (ΔG ≤ −26.16 kJ/mol, ΔH ≥ 31.05 kJ/mol, ΔS ≥ 0.20 kJ/(mol K) showed that the whole CHT adsorption process was spontaneous, and the hydrophobic interaction was predominant. The CHT adsorption capacity of the apple cuticle was higher than that of the red jujube cuticle, potentially due to the significantly higher alkanes content of apples than that of red jujubes. An appropriate ionic strength (0.01 moL/L) could induce a higher adsorption capacity. In addition, the desorption kinetics were shown to conform to a Quasi-first-order model, meaning that not all the adsorbed CHT could be easily desorbed. The desorption ratios in apple and red jujube cuticles were 41.38% and 35.64%, respectively. The results of Fourier-transformed infrared spectroscopy and X-ray photoelectron spectroscopy further confirmed that CHT could be adsorbed and retained in the fruit cuticles. Investigating the adsorption-desorption behavior of CHT in the apple and red jujube cuticles allowed to determine the ratio of its final distribution in the fruits and environment, providing a theoretical basis to evaluate the risk of residue pesticide.

Amine-impregnated natural inorganic nanotubes via layer-by-layer electrostatically self-assembly approach for efficient CO2 adsorption

Developing cost-effective and high-performance solid amine adsorbents has considered as an important way to alleviate the greenhouse effect. How to precisely regulate its pore structure and surface interface characteristics, and how to cooperate to optimize the dynamic mass transfer and adsorption–desorption behavior of gas in the adsorbent are still challenging work. Herein, we demonstrated a facile and efficient approach to construct polyethyleneimine (PEI) impregnated halloysite nanotubes (HNTs) as an emerging nanocomposite for CO2 capture. Based on the natural electrostatic differences of inner and outer walls for HNTs, the hollow tubular structures of adsorbents were constructed by selective surface modification and layer-by-layer electrostatic self-assembly technology to improve the CO2 uptake capacity and cyclic stability, in which poly(sodium-p-styrene sulfonate) (PSS) and PEI were used as polyanionic and polycationic layer, respectively, to coat the inner walls of HNTs. The loading capacity of PSS-PEI composite ionic layers in HNTs and the influence of PSS polyanionic layer on PEI dispersion were specifically discussed according to the CO2 uptake capacity, adsorption heat, thermodynamics and kinetics of the adsorbents. The optimal PEI20-0.5PHNTs adsorbent exhibited a higher CO2 uptake of 0.87 mmol/g at 80 °C in the flow of 40 vol% N2/60 vol% CO2 than that of PEI20-HNTs, owing to the high amine efficiency due to the uniform dispersion of PEI in the electrostatic composite ionic layers. Furthermore, PEI20-0.5PHNTs reached 75 % of the maximum adsorption capacity at the 5th min of the adsorption process and released the most heat during adsorption at − 18.28 kJ/mol due to the presence of electrostatic composite ionic layers. PEI20-0.5PHNTs showed excellent cyclic stability with a slight loss of 7.4 %. The electrostatic self-assembled adsorbent obtained by layer-by-layer loading of PSS and PEI based on the unique surface charge characteristics of HNTs is an inspiration for the synthesis of cost-effective solid amine adsorbents for practical CO2 capture and separation.

Preparation of UiO-66 membrane through heterogeneous nucleation assisted growth strategy for efficient CO2 capture under humid conditions

Metal-organic frameworks (MOFs) have driven the development of polycrystalline membranes in the field of gas separation owing to the strong adsorption-desorption behavior and stable framework structure. However, the poor heterogeneous bonding ability between crystals and the substrate leads to the unsatisfactory gas separation as well as low stability of MOF membranes, especially in the humid environment. Herein, we prepared a thin and defect-free UiO-66 membrane by a crystal heterogeneous nucleation assisted growth strategy for efficient CO2/N2 separation. The addition of small amount of water in the precursor solution promoted the crystal nucleation process on the substrate surface. Meanwhile, the smooth PDMS interlayer guaranteed the heterogeneous well-intergrown of crystals into thin UiO-66 membranes, and provided a hydrophobic environment. Therefore, the dense UiO-66 membrane with a small thickness exhibited a high CO2 permeance (177.4 × 10−9 mol·m−2·s−1·Pa−1) with moderate CO2/N2 selectivity (24.3) under humid conditions. Furthermore, the prepared membrane demonstrated excellent renewable performance after dehumidification at high temperature, and maintained good hydrothermal stability during long-term operation under the humid environment. This work provides a new insight for the design of high-quality MOF membranes and promotes the development of MOF membranes in practical gas separation process.

The effects of co-existing acridine on adsorption-desorption behavior of carbazole in soils: Co-sorption and mechanism insight

Carbazole (CBZ) and acridine (ACR) are polycyclic aromatic nitrogen heterocycles (PANHs) widely found in combined contaminated soils, while investigations on organic-organic interactions have been very limited. In this study, batch experiments were carried out on five soils with different properties, taking CBZ as a representative of PANHs and ACR as a co-existing contaminant. The adsorption isotherms of CBZ (50–1000 μg/L) were nonlinear. Soil organic matter (SOM) and cation exchange capacity (CEC) showed positive correlations with CBZ adsorption-desorption coefficients. The adsorption mechanisms of CBZ involved hydrogen bonding, π-π interaction, and cation-π bonding. Different concentrations of ACR had varying effects on CBZ. The adsorption of CBZ was inhibited with 250 μg/L ACR. The cooperative adsorption was observed on three soils with increasing ACR concentration (1000 μg/L) and led to more pronounced nonlinear isotherms. The S-shaped isotherms of ACR indicated that ACR was adsorbed to the soil surface in a perpendicular configuration. New adsorption sites were created allowing for increased CBZ adsorption through π-π interaction with ACR. Therefore, variations in soil properties and potential impacts of co-existing contaminants should be well considered when assessing the combined pollution of site soil. This will contribute to a more accurate estimation of environmental and health risks.

Upcycle polyethylene terephthalate waste by photoreforming: Bifunction of Pt cocatalyst

Upcycle polyethylene terephthalate (PET) waste by photoreforming (PR) is a sustainable and green approach to tackle environmental problems but with challenges to obtain valuable oxidation products and high purity hydrogen simultaneously. Noble metal cocatalysts are essential to enhance the overall PR reaction efficacy. In this work, TiO2 nanotubes (TiO2 NTs) decorated with single Pt atoms (Pt1/TiO2) or Pt nanoparticles (PtNPs/TiO2) are used in the photoreforming reaction (in one batch), and the oxidation products from ethylene glycol (EG, hydrolysed product of PET) in liquid phase and hydrogen are detected. With Pt1/TiO2, EG is oxidized to glyoxal, glyoxylate or lactate, and hydrogen evolution rate (r H2) reaches 51.8 μmol⋅h−1⋅gcat−1, that is 30 times higher than that of TiO2. For PtNPs/TiO2 (size of Pt NPs: 1.97 nm), hydrogen evolution reaches 219.1 μmol⋅h−1⋅gcat−1, but with the oxidation product of acetate only. DFT calculation demonstrates that for Pt NPs, the reaction path for hydrogen evolution is preferred thermodynamically, due to the formation of Schottky junction. On the oxidation of EG, theoretical and spectroscopic analysis suggest that bidentate adsorption of EG at the interface is facile on Pt1/TiO2, compared to that on PtNPs/TiO2 (two Pt sites), but oxidation products, adsorb less strongly, compared to PtNPs/TiO2, that eventually regulates the distribution of oxidation products. The results thus demonstrate the bifunctions of Pt in the PR reaction, i.e., electron transfer mediator for hydrogen evolution and reactive sites for molecules adsorption. The oxidation reaction is dominated by the adsorption-desorption behavior of molecules but the reduction reaction is controlled by the electron transfer. In addition, acidification of pretreated PET alkaline solution achieves separation of pure terephthalic acid (PTA), which further improves the reaction efficiency possibly by offering high density of active sites and acidic environment. Our work thus demonstrates that to upcycle PET plastics, an optimized process can be reached by atomic design of photocatalysts and proper treatment on the plastic wastes.

Linear enhancement of mechanical compliance by zeolite filling in a compact loudspeaker

A zeolite filling in the rear cavity of a compact loudspeaker enhances the sound pressure amplitude of the loudspeaker system with a frequency range up to ∼500 Hz, but its intrinsic mechanisms remain elusive. We theoretically consider the gas adsorption–desorption behavior on zeolite that can be dynamically perturbed by sound pressure from the diaphragm of the loudspeaker. By merging equivalent circuit theory with gas thermodynamic theory, a linear relationship between mechanical compliance and zeolite volume in the rear cavity is quantitatively modeled. Confirmed by electroacoustic impedance experiments, the linear relationship with a slope of 1.92 mF cm−3 reveals the intrinsic ability of porous material to enhance mechanical compliance by adsorption of gas onto the zeolite in the rear cavity. This study correlates the kinetic behavior of air molecules on zeolite and acoustic behavior; it offers a novel insight to improve the performance of a compact loudspeaker by simple filling with porous material and introduces a comprehensive method for evaluating gas adsorption–desorption dynamics in porous media.

Research Process on the Combined Pollution of Microplastics and Typical Pollutants in Agricultural Soils

As a new type of environmental persistent pollutant， microplastics can not only have adverse effects on the ecosystem but also form complex pollution with co-existing pollutants in the surrounding environment， resulting in higher ecological and health risks. Based on the perspective of agroecosystems， this study focused on the combined pollution of heavy metals， pesticides， and antibiotics， which are three typical pollutants of farmland soil， as well as microplastics and discussed the adsorption-desorption behavior of heavy metals， pesticides， and antibiotics on microplastics. The influence of the structure and properties of microplastics， the physicochemical properties of pollutants， and environmental conditions on the adsorption and desorption behavior of heavy metals， pesticides， and antibiotics on microplastics was discussed. The influence of microplastics on the bioavailability of heavy metals， pesticides， and antibiotics in farmland soil and the internal mechanism were expounded. The existing problems and shortcomings of current research were pointed out， and the future research direction was proposed. This study can provide a scientific reference for ecological risk assessment of the combined pollution of microplastics and typical pollutants in farmland soil.

Adsorption-desorption behavior of florpyrauxifen-benzyl on three microplastics in aqueous environment as well as its mechanism and various influencing factors

Microplastics (MPs) and pesticides are two categories contaminants with proposed negative impacts to aqueous ecosystems, and adsorption of pesticides on MPs may result in their long-range transport and compound combination effects. Florpyrauxifen-benzyl, a novel pyridine-2-carboxylate auxin herbicide has been widely used to control weeds in paddy field, but the insights of which are extremely limited. Therefore, adsorption and desorption behaviors of florpyrauxifen-benzyl on polyvinyl chloride (PVC), polyethylene (PE) and disposable face masks (DFMs) in five water environment were investigated. The impacts of various environmental factors on adsorption capacity were evaluated, as well as adsorption mechanisms. The results revealed significant variations in adsorption capacity of florpyrauxifen-benzyl on three MPs, with approximately order of DFMs > PE > PVC. The discrepancy can be attributed to differences in structural and physicochemical properties, as evidenced by various characterization analysis. The kinetics and isotherm of florpyrauxifen-benzyl on three MPs were suitable for different models, wherein physical force predominantly governed adsorption process. Thermodynamic analysis revealed that both high and low temperatures weakened PE and DFMs adsorption, whereas temperature exhibited negligible impact on PVC adsorption. The adsorption capacity was significantly influenced by most environmental factors, particularly pH, cations and coexisting herbicide. This study provides valuable insights into the fate of florpyrauxifen-benzyl in presence of MPs, suggesting that PVC, PE and DFMs can serve as carriers of florpyrauxifen-benzyl in aquatic environment.

Experimental study of influence of natural organic solvent limonene on methane adsorption–desorption behaviors of selected rank coals

For the clean and efficient extraction of coalbed methane (CBM), it is of great significance to understand the mechanism of the interaction between limonene, which is a natural organic solvent, and coal. In this study, the surface groups, nanoscale pore characteristics, and methane (CH4) adsorption–desorption behaviors of selected rank coals were compared and analyzed to explore the effect of limonene leaching-induced evolution of the macromolecular structure of coal on its adsorption–desorption behaviors. The results showed that with the increase in the mass fraction of limonene, the contents of the aliphatic, aromatic hydrocarbons, and the cross-linking degree of the macromolecular structure of the coal decreased. This led to pore volume expansion of the SH and SQ coals, from a range of 0.3–7 nm to 7–36 nm. The pore volume in the 1.5–7 nm range in the LD coal increased significantly under the combined influence of the pore-expanding effect of the 0.3–1.5 nm pores and the porosity-enhancing effect of the 7–36 nm pores. Therefore, the promotion effect of limonene modification on the CH4 adsorption-desorption behaviors of the coal was more evident in the medium- and high-rank coals than in the low rank-coals.

Distribution and adsorption-desorption of organophosphate esters from land to sea in the sediments of the Beibu Gulf, South China Sea: Impact of seagoing river input

Organophosphate esters (OPEs) have been a class of emerging environmental contaminants. However, studies on their environmental behavior, specifically their adsorption-desorption behavior between sediment and seawater in estuarine and coastal areas, remain limited. To address this gap, our study focused on investigating the levels and behavior of 11 OPEs in sediment samples collected from the Beibu Gulf, South China Sea, encompassing estuaries and coastal regions. The total concentrations of 11 OPEs (Σ11OPEs) in the sediments exhibit a significant decrease in summer, both in seagoing rivers (4.67 ± 2.74 ng/g dw) and the coastal zone (5.11 ± 3.71 ng/g dw), compared to winter levels in seagoing rivers (8.26 ± 4.70 ng/g dw) and the coastal zone (7.71 ± 3.83 ng/g dw). Chlorinated OPEs dominated the sediments, constituting 63 %–76 % of the total. Particularly, port and mariculture areas showed the highest levels of OPEs. Through load estimation analysis, it was revealed that the sedimentary OPEs in Qinzhou Bay (221 ± 128 kg) had the highest load, with input from the Qin River identified as a significant source. Chlorinated OPEs showed a trend of desorption from sediments to the water column with increasing salinity, emphasizing the crucial role of land-based OPEs input through suspended particulate matter in rivers as a pathway to the ocean. The impact of strong flow in estuarine environments was highlighted, as it can scour sediments, generate suspended sediments, and release OPEs into the water bodies. Additionally, the results of the ecological risk assessment indicated that most of the OPEs posed low-risk levels. However, attention is warranted for the contamination levels of some chlorinated OPEs, emphasizing the need for ongoing monitoring and assessment.

Adsorption–desorption behavior of halloysite clay for Cu2+ ions and recovery of copper by electrodeposition method

Halloysite sample, obtained from Phu Tho province, Vietnam, was utilized to investigate the adsorption behavior of Cu2+ ions. Several factors influencing Cu2+ adsorption efficiency and capacity were explored, including pH value, contact time, adsorbent dose, and initial Cu2+ concentration. Under optimal conditions (0.8 g of halloysite per 50 mL of solution, an initial Cu2+ concentration of 40 mg/L, pH 6.2, a contact time of 80 min, and a temperature of 25 °C), the study yielded an adsorption efficiency of 85.19% and a capacity of 2.14 mg/g for Cu2+ ions. Adsorption isotherm analysis was conducted using the Langmuir and Freundlich models, while the kinetics of the adsorption process were investigated through the first-order pseudo and second-order pseudo models. Furthermore, the desorption of Cu2+ ions and the recovery of Cu metal were explored, with a recovery efficiency of Cu reaching 94.65% under suitable conditions (0.3 g mass of halloysite, a current of 7.5 mA, and an electrolytic time of 5 h at 60 °C). These findings suggest the potential application of halloysite clay for removing Cu2+ ions from polluted water, recovering Cu metal, and reusing the adsorbent.

Investigating Oxygen Reduction Performance of Fe-N-C Catalysts for Proton Exchange Membrane Fuel Cells

Non-precious Fe-N-C catalysts have reached high activity levels for acidic oxygen reduction reaction (ORR) in rotating ring disk electrode (RRDE) setup approaching to that of the platinum group metals (PGM) when compared at high catalyst loadings of 0.6-1.0 mgFe-N-C cm-2. The improvements in the ORR activity of Fe-N-Cs can be attributed to new synthetic routes developed in recent years that have led to increased Fe-N4 active site density and utilization and/or better intrinsic activity/turnover frequency (TOF) of those sites.1-3 Despite impressive activities in half-cells, Fe-N-Cs still require quite high loadings in the range of 4.0-5.0 mg cm-2 in proton exchange membrane fuel cells (PEMFCs), which makes the Fe-N-C cathodes 4-5x thicker than Pt-based cathodes (~100 µm for Fe-N-C layer vs ~10-20 µm for Pt layer). Thick Fe-N-C cathodes suffer from quick performance drop in medium to high current density region due to mass-transport related losses. Reducing the Fe-N-C loading levels in RRDE and in PEMFC without comprising the ORR activity would need further improvements in active site density, site utilization and TOF. In this talk, I will present our work on how morphological tailoring of carbon framework in Fe-N-Cs affects the utilization of active sites and water adsorption-desorption behaviour with the aim of improving the ORR performance and mass-transport properties. Active-site imprinted carbon frameworks are used to prepare Fe-N-Cs that consist of purely Fe-N4 sites without any other iron species.1,4,5 Besides activity, performance stability against extensive voltage cycling in RRDE and long-term durability in PEMFC single-cells is another important criterion that Fe-N-Cs need to fulfil for becoming a viable substitute to PGM catalysts. Very recently, encouraging results on the improvement of Fe-N-C durability in PEMFC tests have been reported using radical scavengers and by coating a thin carbon layer on the surface of Fe-N-C.6,7 However, significantly more efforts are required in that direction for reaching the durability targets of thousands of hours. Second part of the talk will discuss the performance stability of Fe-N-Cs.

The effects of Cu-phenanthrene co-contamination on adsorption-desorption behaviors of phenanthrene in soils

Polycyclic aromatic hydrocarbons (PAHs) are persistent organic pollutants in the environment, which are teratogenic, carcinogenic, and mutagenic. Co-contamination of PAHs and heavy metal commonly exists in soil. In this study, 20 types of soils with different properties in China were collected and comprehensively characterized. Phenanthrene (Phe) and Cu (II) were selected as representatives of PAHs and heavy metals, respectively. The adsorption-desorption behaviors of Phe under Phe contamination and Cu (II)-Phe co-contamination in 20 types of soils were studied. The adsorption-desorption behaviors of Phe in 20 types of soils varied greatly, and adsorption of Phe in the soils followed both linear partitioning and nonlinear surface adsorption. Soil organic matter (SOM) plays an important role in the adsorption-desorption behavior of Phe. When the concentrations of Phe were >50 μg/L, soft carbon (SC) fraction of SOM not black carbon (BC) contributed more to the adsorption of Phe. Soil dissolved organic matter (DOM), especially fulvic acid and humic acid fractions, contributes to the adsorption of Phe. Under the effect of Cu (II) (60 mg/L in solution), the adsorption capacity of soil for Phe increased, which possibly resulted from lowered pH, the existence of the cation-π bonding and the "bonding bridge" effect. The systematic investigation of adsorption-desorption behaviors of Phe in soils under heavy metal-PAHs co-contamination will provide a scientific basis for the calculation of soil environmental capacity in the future.

Change in phosphorus availability, fractions, and adsorption-desorption by 46-years of long-term nutrient management in an Alfisol of eastern India

In acid soils, majority of the applied phosphorus (P) transforms to sparingly soluble Fe (PFe) and Al phosphates (PAl), triggering rampant P deficiency. This study aimed to evaluate the impact of long-term (46-years) nutrient management practices on P fractions and P adsorption-desorption behaviour of an acid soil with a soybean-wheat cropping system. Out of ten treatments employed in this experiment, eight most pertinent to the study, viz., control, N (100 % of recommended N fertilizer), NP (100 % of recommended N and P fertilizers), 50 % NPK (50 % of recommended N, P, and K fertilizers), NPK, 150 % NPK, NPK+FYM (100 % of recommended N, P, and K fertilizers with farmyard manure), and NPK+Lime (100 % of recommended N, P, and K fertilizers with lime) were selected. The findings revealed that amorphous Fe and Al, which play a significant role in P fixation, increased due to cultivation. The treatment 150 % NPK recorded the highest available P (104 mg kg-1), followed by NPK+FYM (84.1 mg kg-1) at 0–15 cm depth. The PFe was the dominant inorganic P fraction (25–46 %) while soluble and loosely bound P (the easiest plant available fraction) was the lowest (0.9–1.9 %). The long-term cultivation led to an accumulation of PFe and PAl fractions while caused dissolution of calcium bound P (PCa). The highest content of organic P (Po) was recorded with NPK+FYM (234 kg ha-1). The analysis of Langmuir and Freundlich isotherms indicated that NPK+FYM and 150 % NPK reduced the P adsorption maxima to 341 and 231 mg kg-1, respectively, compared to 406 mg kg-1 for NPK. Moreover, these treatments increased the P sorption saturation to 33 % and 37 %, respectively, as compared to 12 % for NPK, and significantly enhanced P desorption, raising concerns about eutrophication. A path analysis was carried out to elucidate the effects of P dosage, liming, and manuring on soil properties, available P, P adsorption-desorption parameters, yield, and P uptake. In summary, the NPK+Lime treatment offered the most balanced approach, improving both crop yield and P uptake while effectively managing P dynamics in the soil. On the contrary, long-term application of NPK+FYM in an acid soil may result in faster P saturation of adsorption sites and increase the chances of leaching and eutrophication. Furthermore, tailored P fertilization strategies should be developed to better utilize the PFe and PAl fractions and supplementing applied P.

Photo-induced adsorption-desorption behavior of methylene blue on CA-BMO under visible light irradiation.

In this work, the modification of Bi2MoO6 with critic acid (CA-BMO) to achieve enhanced adsorption of methylene blue (MB) solution in dark and desorption under visible light irradiation was reported. The as-prepared materials were synthesized by a hydrothermal method and characterized via SEM, FT-IR, XRD, and XPS techniques. Only 16.5% of 10mg L-1MB was removed within 10min by using 0.5g L-1 Bi2MoO6, while 92.9% removal of MB could be achieved by using 0.5g L-1 CA-BMO, which enhanced the adsorption removal by a factor of 4.6. The adsorption capacity for MB was 18.9mgg-1. Desorption efficiency of MB was only observed in CA-BMO system, and it depends on the wavelength of the light source, pH, and the presence of metal ions. Characterization results suggested that carboxyl groups, which were modified onto the surface of Bi2MoO6, could serve as adsorption sites for MB, and the connections were damaged under light, thus leading to the desorption of MB from the surface of the CA-BMO. This study provides a novel reagent-free desorption strategy for dye recovery without secondary pollution, which facilitates the development and application of Bi-based adsorbent for dye-containing wastewater treatment.

A comparative study of the adsorption and desorption process of selected natural Albanian clays toward methomyl and dimethoate pesticides

Natural soil components, such as clays, have recently piqued interest because of their potential as pesticide adsorbents. This research work sheds light on the possibility of the application of natural Albanian clays as adsorbents for methomyl and dimethoate pesticides from aqueous solutions. Natural Albanian clays from the regions of Brari, Currila, Dardha, and Prrenjasi were employed in the study and were characterized by granulometric analysis and powder X-ray diffraction. Each clay's adsorption capacity and desorption behavior were investigated toward the chosen pesticides. Within 48 h of contact time, methomyl and dimethoate solutions with different concentrations were evaluated at 25 °C to see how the insecticide concentration affected the adsorption & desorption processes for each natural clay type. The experimental data were fitted to Freundlich, Temkin and Dubinin-Radushkevich isotherm like functions and the results showed the best correlation on Freundlich like adsorption isotherm for almost all cases. Brari clay performed better adsorptive properties toward dimethoate, followed by Dardha, Currila and Prrenjasi clays. The dimethoate adsorbed quantities varied from 0.250 mg/g for C = 0.200 g/L to 0.822 mg/g for C = 0.500 g/L. In comparison to Dardha and Prrenjasi clays, Brari and Currila clays exhibit longer saturation times and improved methomyl retention. In the first 2 h of contact, 96.5% of methomyl and 81% of dimethoate were desorbed from Brari clay. The adsorption process was also investigated employing pseudo first-order and pseudo second-order kinetic models, with the results indicating that all clay-pesticide systems studied demonstrated second-order kinetic behavior. Based on the studied desorption process, it is possible to impregnate clays with various insecticides in agriculture and completely control the quantities of the insecticide released.