Organic Inorganic Hybrid Nanocomposites Research Articles

Correction: Dulski et al. An Organic–Inorganic Hybrid Nanocomposite as a Potential New Biological Agent. Nanomaterials 2020, 10, 2551

In the original publication [...]

Synergetic benefits of zinc antimony oxide/reduced graphene oxide hybrid anode for enhanced sodium-ion storage

Organic-inorganic hybrid nanocomposites are rapidly evolving as a new generation of materials with attractive properties for electrochemical energy storage. Unfortunately, their practical applications in sodium-ion batteries (SIBs) still require further research due to the unsatisfactory cycling stability and rate performance. This work explores using zinc antimony oxide/reduced graphene oxide (ZSO/rGO) hybrid nanocomposite as an anode material in SIBs. After 150 cycles at 0.05 A g−1, the ZSO/rGO electrode delivers a specific capacity of 357.21 mAh g−1 with a coulombic efficiency of 99.3 %, which is almost 2.5-fold higher than the specific capacity of the pristine ZSO electrode. An in-situ Raman spectroscopy study demonstrates that the sodiation/desodiation mechanism in the ZSO/rGO electrode involves the conversion and alloying reactions in the ZSO nanoparticles. Further electrochemistry analysis reveals that the nanocomposite anode shows synergistic effects by coupling diffusion and surface contribution, in which the latter plays an important role.

Novel ZnIn2S4/Co(acac)2: An inorganic-organic hybrid nanocomposite for enhanced removal of imidacloprid from aqueous phase

Herein, the synthesis and application of an entirely novel ZnIn2S4/Co(acac)2 (ZIS-Co-2) nanocomposite for degradation of hazardous pesticide imidacloprid (IMD) under visible-light irradiation has been investigated. The ZIS-Co-2 nanocomposite demonstrated an outstanding 97.43 ± 1.84 % removal effectiveness against IMD within 60 min of 23 W LED. This improved catalytic performance was attributable to synergistic effects from ZnIn2S4 doping, which significantly delayed charge recombination and boosted visible-light absorption, promoting efficient photocatalytic degradation. Furthermore, the degradation of IMD was thoroughly verified using chemical oxygen demand (COD), and the total organic carbon (TOC) removal and breakdown mechanism was elucidated using liquid chromatography-mass spectrometry (LC-MS). Notably, the ZIS-Co-2 nanocomposite revealed outstanding recyclability, preserving catalytic activity for up to six cycles and the ability to degrade other emerging contaminants. Furthermore, neither Co(acac)2 nor the combination of ZnIn2S4 with metal complexes has been previously produced or explored for visible light-active photocatalytic applications, highlighting the originality of our study. Overall, the ZIS-Co-2 nanocomposite is a promising and sustainable solution for efficiently removing IMD and other environmental pollutants, with significant practical implications in wastewater treatment and environmental restoration.

Facile fabricated silver Pterocarpus santilinoides biochar-based inorganic–organic hybrid nanocomposite for the photocatalytic decimation of methylene blue and micro-organisms

Facile fabricated silver <i>Pterocarpus santilinoides</i> biochar-based inorganic–organic hybrid nanocomposite for the photocatalytic decimation of methylene blue and micro-organisms

Fabrication of rGO-decorated hBNNS hybrid nanocomposite via organic-inorganic interfacial chemistry for enhanced electrocatalytic detection of carcinoembryonic antigen.

Organic-inorganic hybrid nanocomposites (OIHN), with tailored surface chemistry, offer ultra-sensitive architecture capable of detecting ultra-low concentrations of target analytes with precision. In the present work, a novel nano-biosensor was fabricated, acquainting dynamic synergy of reduced graphene oxide (rGO) decorated hexagonal boron nitride nanosheets (hBNNS) for detection of carcinoembryonic antigen (CEA). Extensive spectroscopic and microscopic analyses confirmed the successful hydrothermal synthesis of cross-linked rGO-hBNNS nanocomposite. Uniform micro-electrodes of rGO-hBNNS onto pre-hydrolyzed ITO were obtained via electrophoretic deposition (EPD) technique at low DC potential (15V). Optimization of antibody incubation time, pH of supporting electrolyte, and immunoelectrode preparation was thoroughly investigated to enhance nano-biosensing efficacy. rGO-modified hBNNS demonstrated 29% boost in electrochemical performance over bare hBNNS, signifying remarkable electro-catalytic activity of nano-biosensor. The presence of multifunctional groups on the interface facilitated stable crosslinking chemistry, increased immobilization density, and enabled site-specific anchoring of Anti-CEA, resulting in improved binding affinity. The nano-biosensor demonstrated a remarkably low limit of detection of 5.47pg/mL (R2 = 0.99963), indicating exceptional sensitivity and accuracy in detecting CEA concentrations from 0 to 50ng/mL. The clinical evaluation confirmed its exceptional shelf life, minimal cross-reactivity, and robust recovery rates in human serum samples, thereby unraveling the potential for early, highly sensitive, and reliable CEA detection.

Synthesis of organic-inorganic hybrid nanocomposites modified by catalase-like catalytic sites for the controlling of kiwifruit bacterial canker.

Kiwifruit bacterial canker, caused by Pseudomonas syringae pv. Actinidiae (Psa), is one of the most important diseases in kiwifruit, creating huge economic losses to kiwifruit-growing countries around the world. Metal-based nanomaterials offer a promising alternative strategy to combat plant diseases induced by bacterial infection. However, it is still challenging to design highly active nanomaterials for controlling kiwifruit bacterial canker. Here, a novel multifunctional nanocomposite (ZnO@PDA-Mn) is designed that integrates the antibacterial activity of zinc oxide nanoparticles (ZnO NPs) with the plant reactive oxygen species scavenging ability of catalase (CAT) enzyme-like active sites through introducing manganese modified polydopamine (PDA) coating. The results reveal that ZnO@PDA-Mn nanocomposites can efficiently catalyze the conversion of H2O2 to O2 and H2O to achieve excellent CAT-like activity. In vitro experiments demonstrate that ZnO@PDA-Mn nanocomposites maintain the antibacterial activity of ZnO NPs and induce significant damage to bacterial cell membranes. Importantly, ZnO@PDA-Mn nanocomposites display outstanding curative and protective efficiencies of 47.7% and 53.8% at a dose of 200 μg mL-1 against Psa in vivo, which are superior to those of zinc thiozole (20.6% and 8.8%) and ZnO (38.7% and 33.8%). The nanocomposites offer improved in vivo control efficacy through direct bactericidal effects and decreasing oxidative damage in plants induced by bacterial infection. Our research underscores the potential of nanocomposites containing CAT-like active sites in plant protection, offering a promising strategy for sustainable disease management in agriculture.

Physicochemical and structural characteristics of hybrid nanocomposites based on branched polyimide with a low content of inorganic component

The series of organic-inorganic hybrid nanocomposites based on branched polyimide matrix and with different amounts of tetraethoxysilane (TEOS) (5, 20, and 50 wt.% of the initial polyamic acid mass) were synthesized and studied using nitroxyl paramagnetic probe, measuring dielectric permittivity, X-ray structural analysis and optical microscopy. It was shown that in some cases the introduction of inorganic component is accompanied by a decrease in the segmental mobility of polyimide matrix as a result of the partial immobilization of organic macrochains during the formation of inorganic microregions. In the presence of inorganic component, a weak dependence of the polymer permeability on the content of the organic component in the system is observed, also the specific density changes little with an increase in TEOS content. Extreme changes in the segmental mobility and dielectric permittivity of the branched matrix formed in the presence of 5 wt% TEOS were found compared to systems of other compositions. This can be caused to a large extent by structural changes in the system. At a low content of TEOS occurs significant «loosening» of organic matrix, a sharp decrease in the dielectric constant and a significant increase in the segmental mobility of the polyimide matrix. Small angle X-ray scattering diffractograms demonstrate drastic changes in polyimide composite heterogeneity in the presence of 5 wt.% TEOS content. According to the optical microscopy data, the introduction of TEOS into polyimide is accompanied by the formation of microaggregates of inorganic nanoparticles in the system, the number and average size of which depend on the SiO2 content and looks most homogeneous at a low TEOS content.

Synthesis and characterization of ureidopyrimidinone-functionalized polyurethane acrylates and their hybrid nanocomposites for UV coating applications

In this study, ureidopyrimidinone moieties (UPy), capable of physical crosslinking via quadruple hydrogen bonding, were successfully incorporated into UV-curable polyurethane acrylate prepolymers. First, a hydroxyl-terminated unsaturated ester monomer was synthesized and reacted with isophorone diisocyanate to create a hydroxyl-terminated UV-curable urethane oligomer (U–OH). Then, isocyanate-terminated building blocks (UPy moieties and an acrylate-based photosensitive monomer) were synthesized and used in various ratios to functionalize U–OH for the preparation of a series of UV-curable UPy-containing polyurethane acrylate (PUA) resins. The resulting products were structurally characterized using 1H NMR and FTIR spectroscopy. Furthermore, organic–inorganic hybrid nanocomposites were obtained by introducing silane coupling agents into PUA resins using the sol–gel process. A series of UV-curable UPy-containing PUA coatings and hybrid nanocomposites were prepared, and their synergistic effect on coating properties was investigated. The dynamic mechanical analysis revealed that the Tg of the samples increased with increasing UPy content, although the mechanical properties remained largely unaltered, as shown by the stress–strain test. The studies also demonstrated that the hybrid nanocomposites exhibited higher decomposition temperatures and better thermal stability compared to pure PUAs. All the coatings exhibited good transparency in the visible region. An optical microscope was used to investigate the self-healing property by scratching the plexiglass panels with a razor blade. Among the other samples, the coating with the highest percentage of UPy content exhibited the best self-healing ability after heat treatment at 90 °C for 10 min.Graphical abstract

Novel highly efficient ternary ZnO wrapped PPy-NTs/g-C3N4 nanocomposite as an epoxy coating for corrosion protection

The main goal of this study is to develop an epoxy coating coupled with an organic–inorganic hybrid nanocomposite that can be used as a corrosion-inhibiting pigment on carbon steel. Herein, polypyrrole nanotubes (PPy-NTs), polypyrrole nanotubes/g-C3N4 (PPy-NTs/g-C3N4) and novel nano-composite polypyrrole nanotubes/g-C3N4/ZnO (PGZ) were prepared by facile wet impregnation approach. The developed pigments were investigated using XRD, FTIR, FE-SEM equipped EDS. Electrochemical impedance spectroscopy (EIS) and polarization measurements were used to assess the behavior of the prepared pigments on the anticorrosion performance of epoxy resin coatings. EIS experiments revealed that introducing nano-pigments to neat coatings enhanced the epoxy resin and charge transfer resistance. The anticorrosion performance of the three nano-pigments was assessed as follows: PGZ ˃ PPy-NTs/g-C3N4˃ PPy-NTs.

Advanced Anticorrosive Graphene Oxide-Doped Organic-Inorganic Hybrid Nanocomposite Coating Derived from Leucaena leucocephala Oil.

Metal corrosion poses a substantial economic challenge in a technologically advanced world. In this study, novel environmentally friendly anticorrosive graphene oxide (GO)-doped organic-inorganic hybrid polyurethane (LFAOIH@GO-PU) nanocomposite coatings were developed from Leucaena leucocephala oil (LLO). The formulation was produced by the amidation reaction of LLO to form diol fatty amide followed by the reaction of tetraethoxysilane (TEOS) and a dispersion of GOx (X = 0.25, 0.50, and 0.75 wt%) along with the reaction of isophorane diisocyanate (IPDI) (25-40 wt%) to form LFAOIH@GOx-PU35 nanocomposites. The synthesized materials were characterized by Fourier transform infrared spectroscopy (FTIR); 1H, 13C, and 29Si nuclear magnetic resonance; and X-ray photoelectron spectroscopy. A detailed examination of LFAOIH@GO0.5-PU35 morphology was conducted using X-ray diffraction, scanning electron microscopy, energy-dispersive X-ray spectroscopy, and transmission electron microscopy. These studies revealed distinctive surface roughness features along with a contact angle of around 88 G.U preserving their structural integrity at temperatures of up to 235 °C with minimal loading of GO. Additionally, improved mechanical properties, including scratch hardness (3 kg), pencil hardness (5H), impact resistance, bending, gloss value (79), crosshatch adhesion, and thickness were evaluated with the dispersion of GO. Electrochemical corrosion studies, involving Nyquist, Bode, and Tafel plots, provided clear evidence of the outstanding anticorrosion performance of the coatings.

Designing an efficient organic–inorganic hybrid nanocomposite for simultaneous oxidative/adsorptive desulfurization of model and real fuel oils

In this study, an efficient organic–inorganic hybrid nanocomposite was designed for deep oxidative/adsorptive removal of dibenzothiophene (DBT) from model and real fuel oils employing surface molecularly imprinted polymer (SMIP) and mesoporous silica nanoparticles (MSNs). On the surface of silanol-functionalized MCM-48-HPW prepared at different 12-tungstophosphoric acid (HPW wt%) as the oxidation catalyst, an imprinted polymethacrylic acid polymer (PMAA) as a selective adsorbent of DBT was formed using different amounts of DBT template. Then, various oxidant/sulfur molar ratios were applied during the desulfurization reactions according to the central composite design (CCD). The successful synthesis of the optimum SMIP-PMAA@MCM-48-HPW nanocomposite was confirmed by FTIR, XRD, N2-adsorption, SEM, TEM, TGA, and NMR techniques. The desulfurization percentage of the model oil reached 98.54% under the optimum conditions, and the catalyst percentage was found to be the most significant parameter for desulfurization efficiency. Comparison experiments showed that the combined role of oxidation and adsorption had an extensive impact on desulfurization efficiency. Under the optimized conditions, 96% DBT from gasoline was removed by the optimum nanocomposite. The optimum nanocomposite showed good stability and could be reused five times without a remarkable decrease in the desulfurization ability.

Customized Microenvironments Spontaneously Facilitate Coupled Engineering of Real-Life Large-Scale Clean Water Capture and Pollution Remediation.

Harnessing abundant renewable resources and pollutants on a large scale to address environmental challenges, while providing sustainable freshwater, is a significant endeavour. This study presents the design of fully functional solar vaporization devices (SVD) based on organic-inorganic hybrid nanocomposites (CCMs-x). These devices exhibit efficient photothermal properties that facilitate multitargeted interfacial reactions, enabling simultaneous catalysis of sewage and desalination. The localized interfacial heating generated by the photothermal effect of CCMs-x triggers surface-dominated catalysis and steam generation. The CCMs-x SVD achieves a solar water-vapor generation rate of 1.41kg m-2 h-1 (90.8%), and it achieves over 95% removal of pollutants within 60min under one-sun for practical application. The exceptional photothermal conversion rate of wastewater for environmental remediation and water capture is attributed to customized microenvironments within the system. The integrated parallel reaction system in SVD ensures it is a real-life application in multiple scenarios such as municipal/medical wastewater and brine containing high concentrations. Additionally, the SVD exhibits long-term durability, antifouling functionality toward complex ionic contaminants. This study not only demonstrates a one-stone-two-birds strategy for large-scale direct production of potable water from polluted seawater, but also opens up exciting possibilities for parallel production of energy and water resources.

Preparation of thermally stable organic-inorganic hybrid nanocomposites from chemically functionalized oxidized graphite by in situ catalytic oxidative decarboxylation

ABSTRACT In this study, the preparation of thermally stable organic-inorganic hybrid nanocomposites from chemically functionalized oxidized graphite is carried out by in-situ catalytic oxidative decarboxylation of 3,5-dinitrobenzoic acid (reactant) in the presence of potassium persulfate (oxidant), silver nitrate (catalyst) and graphite (support) under thermal or microwave conditions. The effects of heat transfer and dosages of reactant, catalyst and oxidant on the crystalline structure and the morphology of nanocomposites are studied in detail. The prepared nanocomposites are characterized by EDS, elemental mapping, FE-SEM, FT-IR and XRD. The thermal stability of nanocomposites is examined by TGA and DSC. EDS shows that nanocomposites are composed of C, O, N, S, K and Ag elements. FT-IR exhibits that the graphitic layers in nanocomposites are mainly oxidized and functionalized with carboxyl, carbonyl, hydroxyl, epoxy, sulfate, nitrate and nitroaryl groups. Addition of nitroaryl groups to nanocomposites is also supported by an increase found in their C and N contents. XRD demonstrates the coexistence of both oxidized amorphous carbon and graphite in combination with different levels of organic and inorganic phases. The prepared nanocomposites show good thermal stability. The total area of the DSC curve in these nanocomposites compared to graphite is enhanced.

Development of sustainable polybenzoxazine-based organic–inorganic hybrid nanocomposites for high voltage insulator applications

Development of sustainable polybenzoxazine-based organic–inorganic hybrid nanocomposites for high voltage insulator applications

Active-site-rich binary metal oxides integrated organic–inorganic hybrid nanocomposite: Electrochemical simultaneous detection of multi-drugs of isoprenaline and resorcinol in real samples

In recent years, awareness on human health is increasing, which also increased the use of drugs to efficiently cure or halt the disease. Besides their certain beneficiary effects, it also triggers some alarming conditions in the body when the drug crosses a certain limit. Therefore, there is a need to develop efficient methods to detect the amount of the drug in the human body. In this work, for the first time, we developed a novel zinc manganate incorporated on polydopamine encapsulated reduced graphene oxide hybrid nanocomposite (rGO-pDA-ZnMnO3 HNC) efficient electro-catalyst for the simultaneous electrochemical detection of multi-drugs of Isoprenaline (IP) and Resorcinol (RC). The incorporation of the ZnMnO3 on rGO-pDA sheets indicates excellent conductivity due to its enhanced active sites and high surface area. The rGO-pDA-ZnMnO3 HNC was drop-casted on the surface of GCE and used as a superior electro-catalyst for individual and simultaneous detection of multi-drugs using CV and DPV. The DPV results showed excellent electrochemical performance, like IP and RC in linear ranges (LR) of 0.004 – 85.99 and 0.04 – 27.9 µM and lower limit values (LOD) of 3.1 and 7.1 nM, respectively. Further, the modified GCE has excellent interference capability, repeatability, and stability. Finally, the practical impact was demonstrated in real-time samples of human urine, tap water, and hair dyes. Remarkably, the recovery rate of IP and RC is ∼99 % and ∼98 %, respectively with RSD of less than 3 %, which authenticates the usefulness of the proposed sensor for real-time applications.

Multifunctional Architectures of Cyclic Dipeptide Copolymers and Composites, and Modulation of Multifaceted Amyloid-β Toxicity.

Alzheimer's disease (AD) is a major neurodegenerative disorder primarily characterized by the β-amyloid (Aβ42) misfolding and aggregation-associated multifaceted amyloid toxicity encompassing oxidative stress, neuronal death, and severe cognitive impairment. Modulation of Aβ42 aggregation via various structurally anisotropic macromolecular systems is considered effective in protecting neuronal cells. In this regard, we have developed a cyclic dipeptide (CDP)-based copolymer (CP) and explored its material and biomedical properties. Owing to the structural versatility, CDP-CP forms solvent-dependent anisotropic architectures ranging from dense fibers and mesosheets to vesicles, which are shown to interact with dyes and nanoparticles and mimic synthetic protocells, providing a conceptually new approach to achieve advanced functional materials with the hierarchical organization. CP upon interaction with gold nanoparticles (GNP) and polyoxometalate (POM) generated faceted architectures (CP-GNP) and the nanocomposite (CP-POM), respectively. CP-GNP and CP-POM have shown remarkable ability to inhibit Aβ42 aggregation, dissolve the preformed aggregates, and scavenge reactive oxygen species (ROS) to ameliorate multifaceted amyloid toxicity. In cellulo studies show that CP-GNP and CP-POM protect neuronal cells from Aβ42-induced toxicity and reduce lipopolysaccharide (LPS)-activated neuroinflammation at sub-micromolar concentration. To our knowledge, this is the first report on the hierarchical organization of CDP-CP into 1D-to-2D architectures and their organic-inorganic hybrid nanocomposites to combat the multifaceted amyloid toxicity.

New organotin(IV) complexes with a bis-acyl-hydrazone ligand: Synthesis, crystal structure and immobilization on magnetic mesoporous silica nanoparticles as a strategy in cancer therapy

The new binuclear organotin(IV) complexes, (Me2Sn)2L (1) and (Ph2Sn)2L (2), have been synthesized from reaction of R2SnCl2 (R = Me or Ph) with bis(2-hydroxy-1-naphthaldehyde) Succinic dihydrazone (H4L). The synthesized compounds have been characterized by elemental analysis and IR, 1H NMR, and 119Sn NMR spectroscopy. The structures of 1 have been also determined by X-ray crystallography. Both complexes are binuclear with bis-hydrazone coordinated via enolic and phenolic oxygens and imine nitrogen in two tridentate ONO domains. Dihydrazone ligand and its diphenyltin(IV) complex were also chemically immobalized on functionalized magnetic mesoporous silica nanoparticles. The new organic-inorganic hybrid nanocomposites were characterized by FT‐IR, PXRD, BET, TGA, VSM, FE‐SEM, HRTEM and EDX techniques. Then, the in vitro cytotoxicity of the synthesized compounds against A549 cancer cell lines was evaluated. Diphenyltin(IV)-loaded magnetic mesoporous silica nanoparticles, Fe3O4@mSiO2-SnPh2, displayed the highest cytotoxic activity compared to other nanoparticles and also was able to reduce the cell viability in a more efficient manner in comparison with the free (Ph2Sn)2L. The inverted microscopy morphology and acridine orange staining indicate that A549 cells progress to cell death after being treated with Fe3O4@mSiO2-SnPh2 nanoparticles.

Organic–inorganic hybrid nanocomposites for the photoreduction of CO2: environment and energy technologies

Organic–inorganic hybrid nanocomposites for the photoreduction of CO2: environment and energy technologies

Engineering the Properties of Transparent Hybrid Coating toward High Hardness, Excellent Flexibility, and Multifunction.

Transparent functional coatings with glass-like hardness and polymer-like flexibility are highly desirable for flexible and foldable displays. Although several coatings have been developed toward this goal, achieving a functional coating with 9H pencil hardness and extremely low bending radius of curvature (rc) remains a great challenge due to the inherent conflict between hardness and flexibility. To overcome this trade-off, a facile strategy is developed herein. The coating is an organic-inorganic hybrid nanocomposite that is prepared from thiol-acrylate polymerization of acrylo polyhedral oligomeric silsesquioxane and multifunctional thiols. The former provides the desired hardness, while the latter affords high flexibility and the maximum level of chemical bonding for organic-inorganic phases. Because of the good miscibility and varied functionality of monomers, we are able to manipulate the composition and internal structure of coating systematically, endowing it with high transparency (98%, 550 nm), super hardness (9H), excellent low modulus (1.85 GPa, the most flexible one to date), and the ability to withstand steel wool's abrasion and repeated bending (rc = 0.8 mm) 10 000 times on PET film. On the final coating, both antifouling and antibacterial abilities are integrated without sacrificing its other properties after postfunctionalizing a zwitterionic layer. This work balances the hardness-flexibility conflict effectively and provides some useful protective coatings for next-generation displays.

Experimental Insights into Mesoporous Polyaniline-Based Nanocomposites for Anionic and Cationic Dye Removal.

This work presents the preparation of inorganic-organic hybrid nanocomposites, namely three-dimensional polyaniline (Pani)/activated silica gel (ASG) (3D Pani@ASG), their characterization, and in removing application as a potential adsorbent for cationic brilliant green (BG), crystal violet (CV), and anionic Congo red (CR), and methyl orange (MO) dyes. Pani@ASG nanocomposites have been prepared by the in situ polymerization method and characterized using various techniques such as Fourier transform infrared (FTIR), X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM) with selected area electron diffraction, thermogravimetric analysis with derivative thermogravimetry, zeta potential analyses, and Brunauer-Emmett-Teller (BET). The scanning electron microscopy (SEM) study confirms the average particle size of the Pani@ASG nanocomposite is in the range of 5 nm. FESEM, TEM, FTIR, and XRD analysis proved the successful decoration of ASG over Pani. The BET result of Pani@ASG shows a mesoporous nature with a pore diameter of less than 3 nm and a surface area of 423.90 m2 g-1. Both SEM and TEM analyses show the proportional distribution of ASG over Pani's surface. The adsorption trend of BG and MO on the studied materials at pH 7 was found as follows: Pani@ASG > Pani > ASG. The highest sorption capacities of MO and BG on Pani@ASG were 161.29 and 136.98 mg/g (T = 298.15 K, and Pani@ASG dose: 0.04 g for MO and 0.06 g for BG), which were greater compared with bare Pani and bare ASG, respectively. The interaction mechanism behind the adsorption of BG and MO dyes onto the Pani@ASG nanocomposite includes electrostatic interaction, π-π interaction, and hydrogen bonding. The mechanistic pathway and the interactions between the targeted dyes and Pani@ASG were further studied using adsorption isotherm, adsorption kinetics, and thermodynamics.