New Coccine Research Articles

The self-boosting ultrafast removal of Cr(VI) and organic dye in textile wastewater through sulfite-induced redox processes

The treatment of textile wastewater containing harmful metal ions poses a significant challenge in industrial applications due to its environmental impact. In this study, the use of sulfite for treating simulated dye wastewater containing New Coccine (NC) and Cr(VI) was investigated. The removal of NC was influenced by the redox reaction between Cr(VI) and sulfite, demonstrating a strong self-boosting effect of Cr(VI) on NC removal. Remarkable NC decoloration (95%) and Cr(VI) reduction (90%) were achieved within 1 min, highlighting the effectiveness of the treatment. Quenching experiments and electron paramagnetic resonance (EPR) technology confirmed that singlet oxygen (1O2) was the main oxidative agent for organic dye removal and SO4•−, •OH and Cr(V) were also identified as key contributors to NC degradation. The Cr(VI)/sulfite system exhibited higher efficiency in degrading azo dyes, such as NC and Congo Red (CR), compared to non-azo dyes like Methylene Blue (MB). This superiority may be attributed to the action of Cr(V) on azo groups. Additionally, the COD removal experiments were conducted on the actual dye wastewater, showing the excellent performance of the Cr(VI)/Sulfite system in treating industrial textile wastewater. This approach presents a promising strategy for effective “waste control by waste”, offering great potential for addressing challenges related to dye wastewater treatment and environmental pollution control in practical industrial scenarios.

Highly efficient and selective removal of anionic dyes from aqueous solutions using polyacrylamide/peach gum polysaccharide/attapulgite composite hydrogels with positively charged hybrid network

To avoid the weakness (lower adsorption rate and selectivity) of peach gum polysaccharide (PGP) and improve the adsorption performance of polyacrylamide (PAAm) hydrogel (lower adsorption capacity), in the present work, the PGP was chemically tailored to afford ammoniated PGP (APGP) and quaternized PGP (QPGP), and attapulgite (ATP) was bi-functionalized with cation groups and carbon‑carbon double bond. Then, PAAm/APGP and PAAm/QPGP/ATP hydrogels were synthesized via redox polymerization. The synthesis procedure and properties of hydrogels were traced by FTIR, SEM, XPS, TGA, TEM, and BET methods, and the dye adsorption performance of the hydrogels was evaluated using the new coccine (NC) and tartrazine (TTZ) aqueous solutions as the model anionic dyes. Effects of initial dye concentration, pH, and ionic strength on the adsorption were investigated. Compared with PAAm/APGP hydrogel, PAAm/APGP/ATP hydrogel exhibits higher adsorption rate, superior adsorption capacity, stability, and selectivity towards anionic dye. The adsorption process of PAAm/QPGP/ATP hydrogel reached equilibrium in about 20 min and followed the pseudo-second-order kinetic model and Langmuir isotherm. The adsorption capacities towards NC and TTZ of PAAm/QPGP/ATP hydrogel were calculated as 873.235 and 731.432 mg/g. This hydrogel adsorbent originating from PAAm, PGP, and ATP shows great promise for application in practical water treatment.

Fluorescent composite based on peptide nanotubes activating coumarin 6 for sensitive detection of new coccine in food samples

New coccine (NC), as a kind of common colorant, has been frequently used in our daily life. Herein, the fluorescent composite (PNTs@C6) prepared by the hydrophobic non-covalent interaction between peptide nanotubes and coumarin 6 (C6) was designed for the determination of NC. Due to the activation of C6 by peptide nanotubes, the composite exhibits strong green fluorescence emission, which can be selectively quenched by NC through the inner filter effect. Therefore, a new fluorescent method based on the PNTs@C6 composite for NC detection was constructed. Under optimal conditions, the fluorescence quenching of the sensor exhibits a good linear relationship with the concentration of NC in the range of 0.01–10 μM and the limit of detection is 3.6 nM. Furthermore, the strategy shows simplicity, rapid response and high selectivity and has been successfully applied to the detection of NC in food samples.

Multivalent iron-based magnetic porous biochar from peach gum polysaccharide as a heterogeneous Fenton catalyst for degradation of dye pollutants

Water contamination caused by organic dyes has become a significant concern, and catalytic degradation of dye pollutants is an effective solution. However, developing an affordable, easy-to-prepare, high-catalytic-activity, and renewable catalyst has proved challenging. The current study addresses this issue by introducing an efficient heterogeneous Fenton catalyst, known as multivalent iron-based magnetic porous biochar (mFe-MPB). This catalyst comprises multiple iron species, such as Fe3O4, γ-Fe2O3, zero-valent Fe (Fe0), and Fe3C. The mFe-MPB was easily prepared by utilizing a straightforward crosslinking-pyrolysis strategy with natural peach gum polysaccharide (PGP), which has a unique structure and composition that facilitates the creation of multivalent iron species. The mFe-MPB demonstrates high catalytic activity in the degradation of an array of dyes, including cationic dyes such as methylene blue (MB) and methyl violet (MV), as well as anionic new coccine (NC) dye. Its mass standardized rate constant value for catalytic degradation of MB can reach as high as 1.65 L min−1 g−1. Additionally, the catalyst can be easily recovered through magnetic separation and possesses remarkable structural stability, enabling several reuses without compromising its efficiency. Therefore, this study offers a viable strategy to fabricate low-cost, efficient and sustainable Fenton catalyst for removal of dye pollutants from water.

Aggregation-induced bimodal excitation of nitrogen-doped carbon dots for ratiometric sensing of new coccine and solid-state multicolor lighting

Trace detection of foodstuff pigments have gained increasing attention because of their close association with biological and environmental processes. Herein, we propose an innovative bimodal excitation nitrogen-doped carbon dots (N-CDs) for ratiometric sensing of new coccine (NC) pigment, which are synthesized by using melamine and o-phenylenediamine as precursors via solvothermal treatment. With the increase of the N-CDs concentration, N-CDs exhibit not only a concentration-dependent tunable color behavior, but also a novel aggregation-induced bimodal excitation phenomenon. Considering this distinctive bimodal excitation behavior, a ratiometric sensor based on N-CDs has been developed for the detection of the NC in different organic solvents due to the inner filter effect and fluorescence resonance energy transfer. The intensity ratio of two excitation signals is linear with the NC concentration in the range of 0.032–100 µM, and the limit of detection is as low as 32.1 nM. Meanwhile, we realize the design of multicolor-emission N-CDs/polymer films. All in all, this work presents a novel kind view of the mechanism of distinctive bimodal excitation of N-CDs, and further proposes an innovative ratiometric method for the screening analysis of NC in food samples and environmental pollutants.

Bright orange-emissive carbon quantum dots as an ultrasensitive nanoprobe for new coccine determination in food samples

In this study, an ultrasensitive fluorescence method based on bright orange-emissive carbon quantum dots (OE-CQDs) was for the first time developed for the detection of new coccine (NC). The OE-CQDs were synthesised by a one-pot solvothermal method with saffron T as precursor. The detection mechanism was based on the interaction between OE-CQDs and NC, where the fluorescence of OE-CQDs was inhibited by NC via inner filter effect (IFE) and static interaction. The OE-CQDs probe exhibited high selectivity and good anti-interference ability towards NC sensing. A linear relationship with the concentration of NC in a range of 0.01–20.0 µmol L−1 and a detection limit as low as 1.8 nmol L−1 were obtained. The developed fluorescence method was successfully applied for NC determination in commercial food samples, including dried waxberry, haw flakes, watermelon frost lozenges, strawberry jam and energy drink, with satisfactory results were achieved. The recoveries were in a range of 97.0–104.0% and the relative standard deviations (RSDs) were less than 3.74%. This work highlights the great potential of using long-wavelength emissive CQDs as nanoprobe to achieve enhanced sensitivity in food additives sensing.

Green fabrication of citrus pectin-Ag@AgCl/g-C3N4 nanocomposites with enhanced photocatalytic activity for the degradation of new coccine

In this research, novel citrus-pectin-based Ag@AgCl/graphite carbon nitride nanocomposites (CACNs) were formed by assembling citrus-pectin-based Ag@AgCl (CP-Ag@AgCl) prepared by daylight-driven reduction onto a graphite carbon nitride (g-C3N4) surface. The as-prepared samples were characterized by various techniques to study their morphology, structure, optical and electrochemical properties. The CACNs were found to have enhanced photoelectrochemical properties, which provided excellent photocatalytic activity to degrade the food colorant new coccine (NC) under visible light. For the NC degradation, the recommended photocatalyst offered approximately 95.7% of the degradation efficiency under visible-light irradiation for 60 min, which has superior photostability and reusability. Its degradation rate constant was approximately 5.16 and 37.6 times those of pure g-C3N4 and CP-Ag@AgCl, respectively. The NC degradation conformed to pseudo-first-order kinetics. Thus, the developed nanocomposites provide a useful reference for the removal of hazardous food colorants and resource utilization of peel waste.

Adsorptive Removal of Azo Dye New Coccine Using High-Performance Adsorbent-Based Polycation-Modified Nano-Alpha Alumina Particles.

The azo dyes new coccine (NCC) were successfully removed through the adsorption onto PVBTAC-modified α-Al2O3 particles. The optimal conditions of both the surface modification by PVBTAC adsorption and the NCC adsorption were thoroughly investigated. Formerly, polycations PVBTAC were adsorbed onto the nanosized α-Al2O3 particles at pH 8, NaCl 100 mM, with a contact time of 2 h, and initial concentration of 1000 ppm to modify the α-Al2O3 surface. Latterly, the NCC adsorptive removal was conducted at pH 8, NaCl 10 mM, α-Al2O3 adsorbent dosage of 3 mg mL−1, and a contact time of 45 min. Interestingly, the optimal pH of 8 potentially applies to treat real wastewater as the environmental pH range is often about 7–8. High removal efficiency and adsorption capacity of the NCC azo dyes were, respectively, found to be approximately 95% and 3.17 mg g−1 with an initial NCC concentration of 10 ppm. The NCC adsorption on the modified α-Al2O3 particles was well fitted with a Freundlich model isotherm. A pseudo-second kinetic was more suitable for the NCC adsorption on the PVBTAC-modified α-Al2O3 surface than a pseudo-first kinetic. The NCC adsorptive removal kinetic was also affirmed by the FT-IR spectra, based especially on the changes of functional group stretch vibrations of −SO3− group in the NCC molecules and −N+(CH3)3 group in the PVBTAC molecules. The high reusability of the α-Al2O3 particles was proved to be higher than 50% after four generation times.

Adsorptive Removal of Anionic Azo Dye New Coccine Using Silica and Silica-gel with Surface Modification by Polycation.

In the present work, adsorption of anionic azo dye, new coccine (NCC) on silica and silica-gel in an aquatic environment was discovered. Effective conditions such as adsorption time, pH, the influence of dosage on NCC adsorption using strong polycation, poly-diallyl-dimethylammonium chloride (PDADMAC) modified silica (PMS) and PDADMAC modified silica-gel (PMSG) were systematically studied. The removal of NCC using PMS and PMSG were much higher than that using raw silica and silica-gel without PDADMAC in all pH ranges from 3 to 10. The adsorption of NCC onto PMS and PMSG was achieved maxima at the same conditions of contact time 30 min, pH 6. The optimum adsorbent dosages of PMS and PMSG for NCC removal were 10 and 20 mg·mL−1, respectively. Experimental results of NCC adsorption isotherms onto PMS and PMSG at different ionic strength were fitted by Langmuir and Freundlich models. The NCC removal efficiencies using PMS and PMSG were higher than 87%, indicating that PMS and PMSG are novel and reusable adsorbents for removal of anionic dye. Based on adsorption isotherms, and surface group changes after PDADMAC modification and NCC adsorption examined by Fourier transform infrared spectroscopy (FTIR), we demonstrate that electrostatic interaction between positively charged adsorbents’ surfaces and negative sulfonic groups of NCC are the main driving force for anionic azo dye adsorption onto PMS and PMGS adsorbents.

Innovative baffled microbial fuel cells for azo dye degradation: Interactive mechanisms of electron transport and degradation pathway

Two membrane-less baffled microbial fuel cells (BMFCs) were developed for non-dye (BMFC1) and dye degradation (BMFC2) investigations along with simultaneous bioelectricity generation. The influence of salinity, organic loading, circuit connection, aeration rate, dye concentration and addition of intermediates on BMFCs performances were evaluated systematically. The increase of salinity by 3-fold (0.39 g/L of NaCl) lowered the internal resistance of BMFC1 system by 38%–620 Ω, and the power density increased 49% to 10.55 ± 0.86 mW/m2. While the further increase of salinity (10-fold) adversely affected BMFC1. The power performance of BMFC1 improved with higher organic loading. Whereas, the increment in organic loading enhanced the decolourisation efficiency but deteriorated the power performance of BMFC2 ascribed to the competition between New Coccine (NC) molecules and anode for electrons. This finding corroborates that NC was a preferable electron acceptor than the anode. The addition of 50 mg/L NC increased the power density by 53% to 12.40 ± 1.60 mW/m2, which revealed that NC decolourised intermediates could act as the electron mediator, hence led to the increase of power performance. The electron-mediating mechanism of NC decolourised intermediate, 1-amino-2-naphthol-6,8-disulfonate as electron shuttle was unveiled. The in-depth understanding of the mechanisms involved in dye degradation in MFCs was presented, where a comprehensive degradation pathway of NC was proposed based on the intermediates identified via UV–Visible spectra, Fourier-transform infrared spectroscopy (FTIR), high-performance liquid chromatography (HPLC) and gas chromatograph-mass spectrometer (GC-MS) analyses.

Preparation of Stable Hydrophilic Polyethyleneimine Cross-Linked Graphene Oxide/Titanium Dioxide Membranes for Dye Separation

An excellent novel laminar and hierarchical polyethyleneimine cross-linked graphene oxide/titanium dioxide (GO–TiO2–PEI) membrane was successfully prepared by vacuum filtration technology using polyethyleneimine (PEI) as the cross-linking agent and a GO–TiO2 nanocomposite as the substrate. The resultant membrane (GO–TiO2–PEI) displayed a favorable antifouling performance with bovine serum albumin (BSA) and showed good hydrophilicity and wettability, with a static water contact angle of 13.2∘. The stability of the GO–TiO2–PEI membrane in aqueous solution obviously improved with the cross-linking of PEI compared with that of the GO and GO–TiO2 membranes. The GO–TiO2–PEI membrane also exhibited a satisfactory water flux of 48.6[Formula: see text]L m[Formula: see text] h[Formula: see text] bar[Formula: see text]. The GO–TiO2–PEI membrane exhibited a good performance for effectively separating different dyes including methylene blue (MB), rhodamine B (RB), methyl orange (MO), sunset yellow (SY), new coccine (NC) and amaranth. All the above results suggested that the GO–TiO2–PEI membrane could be used as an excellent stable hydrophilic membrane for efficiently separating dyes from aqueous solution.

Plasmonic nanoparticles on metal-organic framework: A versatile SERS platform for adsorptive detection of new coccine and orange II dyes in food

Synthetic dyes have been widely applied to food processing, but abuse of colourants in food may pose risks to human health. To analyze new coccine (NC) and orange II (OII) in food, a versatile surface-enhanced Raman scattering (SERS) platform was proposed. A metal-organic framework (MOF, UiO-66(NH2)) with octahedral crystal structure was synthesized and gold nanoparticles were grown on the MOF surface to fabricate UiO-66(NH2)@Au versatile SERS platform. The UiO-66(NH2)@Au displayed much better SERS performance than gold nanoparticles with high R2 of 0.9684 for NC and 0.9912 for OII and low LOD of 0.4015 mg/L for NC and 0.0546 mg/L for OII. The recoveries of NC and OII in Mirinda soft drink and paprika ranged from 82.92 to 109.63%. This study provided a sensitive and rapid method for determination of NC and OII through UiO-66(NH2)@Au, and the proposed SERS platform revealed great potential for analyzing synthetic colourants in food samples.

Enhanced photocatalytic New Coccine degradation and Pb(II) reduction over graphene oxide-TiO2 composite in the presence of aspartic acid-β-cyclodextrin

In this work, aspartic acid-β-cyclodextrin (ACD) was synthesized by the reaction of β-cyclodextrin with aspartic acid and epichlorohydrin, and graphene oxide-TiO2 (GO-TiO2) composite catalyst was prepared by a hydrothermal method. The complexation of ACD with New Coccine (NC) and Pb2+ was characterized with FT-IR and XPS, respectively, the results show that ACD can simultaneously complex NC and Pb2+. XRD analysis and SEM images of GO-TiO2 show that TiO2 platelets are well distributed on both sides of the graphene oxide sheets, and display a similar XRD pattern to the pure TiO2 nanoparticles with the typical diffraction peak of anatase phase. The effects of ACD on the photocatalytic degradation of NC and photocatalytic reduction of Pb2+ were investigated in the single pollution system, and the synergistic effects on the simultaneous photocatalytic NC degradation and Pb2+ reduction in the presence of ACD were also evaluated. The results showed that the presence of ACD was favorable to the acceleration of photocatalytic oxidation of NC and photocatalytic reduction of Pb2+ in the single pollution system, and the photocatalytic reaction rate constants of NC and Pb2+ in the presence of ACD increased 58% and 42%, respectively. For the combined pollution system, the synergistic effects on the simultaneous conversion of NC and Pb2+ in aqueous solutions were also further enhanced. ACD enhanced photocatalytic activity was attributed to the improvement of the electron transfer and mass transfer at the GO-TiO2 interface.

NADH-fluorescence absorption correction to determine absolute fluorophore concentrations of a liquid tissue model

Fluorescence emission intensity is an important indicator for characterising tissue. This study extends our previous work and presents an algorithm to determine the absolute nicotinamide adenine dinucleotide hydrate (NADH) concentration of a liquid tissue model with the aid of a multispectral needle probe. Besides the scattering correction, this newly developed algorithm has the ability to compensate the absorbance effects of the tissue model. As an absorber new coccine (NC) is used to mimic the haemoglobin’s absorbance of human tissue, while Calcilit imitates the tissue’s scattering. The algorithm’s bases are the differences between two definite integrals of the absorbance remission and the fluorescence emission spectrum, respectively. Using this simple mathematic model, an algorithm to determine NADH concentrations between 0.5 and 2.0 mM at 2.7 wt% Calcilit and NC concentrations between 0.252 and 2.520 mM is successfully tested. This results in a mean absolute percentage error (MAPE) of 0.3% for the calculation of the Calcilit concentration and MAPEs of 3.3 and 5.0% to determine the fluorophore concentration.

Disclosing the synergistic mechanisms of azo dye degradation and bioelectricity generation in a microbial fuel cell

Microbial fuel cell (MFC) with cost-effective aerobic biocathode was developed for further treatment of azo dye intermediates into less harmful products in a single system. The fate of electrons in MFC for azo dye decolourisation and bioelectricity generation were explored via a series of studies including the effects of azo dye concentration, organic loading, external resistance and hydraulic retention time. The addition of low concentration of New Coccine (NC) (25 mg/L) improved 17% of the power density to 20.13 ± 0.37 W/m3. The internal resistance decreased from 50 to 32 Ω. As dye concentration increases, the decolourisation efficiency maintained over 90% (200 mg/L NC), whereas, power density dropped to 10.83 ± 1.21 W/m3. The increase of NC to higher concentration hindered the bioelectricity production, as both anode and azo dye molecules were competing for electrons. More electrons were utilized for decolourisation than bioelectricity generation as decolourisation efficiency improved, but power density dropped with the increase of organic loading. Lower external resistance allowed greater electron transfer, thus it enhanced the overall power performance. Higher power density (15.12 ± 1.12 W/m3) and normalized energy recovery (76 Wh/kg COD) were achieved at the lowest external resistance of 100 Ω. Both decolourisation and power performances were improved with 2 days HRT. The intermediate products from decolourisation and mineralization processes were identified, and the degradation pathway of NC has been proposed based on the UV–Vis, HPLC and GC–MS results.

COMPARISON ON SOLAR PHOTOCATALYTIC DEGRADATION OF ORANGE G AND NEW COCCINE USING ZINC OXIDE AS CATALYST

The mineralization of azo dyes could be realized through solar photocatalytic degradation that is a green method where non-harmful end products are produced. The aim of this study was to investigate the mineralization of Orange G (OG) and New Coccine (NC) using ZnO as catalyst. The degradation of the azo dyes was conducted at different experimental conditions, and parameters such as effect of sunlight to the degradation rate, initial azo dye concentration, amounts of catalyst dosage, pH and effect of aeration to the decolorization of azo dye were investigated. Photocatalytic mineralization of the azo dyes was evaluated through the analysis of UV-Vis spectra, chemical oxygen demand (COD) and ion chromatography (IC) for residual ionic species analysis. The results showed that solar photocatalytic degradation using ZnO was effective for colour removal and the photodegradation rate followed Langmuir-Hinshelwood kinetic model. It was observed that the degradation rate of NC was higher than OG which may be due to the different number of sulphonate ions that are attached on to the azo dye molecule.

Microbial fuel cell operation using monoazo and diazo dyes as terminal electron acceptor for simultaneous decolourisation and bioelectricity generation

Monoazo and diazo dyes [New coccine (NC), Acid orange 7 (AO7), Reactive red 120 (RR120) and Reactive green 19 (RG19)] were employed as electron acceptors in the abiotic cathode of microbial fuel cell. The electrons and protons generated from microbial organic oxidation at the anode which were utilized for electrochemical azo dye reduction at the cathodic chamber was successfully demonstrated. When NC was employed as the electron acceptor, the chemical oxygen demand (COD) removal and dye decolourisation efficiencies obtained at the anodic and cathodic chamber were 73±3% and 95.1±1.1%, respectively. This study demonstrated that the decolourisation rates of monoazo dyes were ∼50% higher than diazo dyes. The maximum power density in relation to NC decolourisation was 20.64mW/m2, corresponding to current density of 120.24mA/m2. The decolourisation rate and power output of different azo dyes were in the order of NC>AO7>RR120>RG19. The findings revealed that the structure of dye influenced the decolourisation and power performance of MFC. Azo dye with electron-withdrawing group at para substituent to azo bond would draw electrons from azo bond; hence the azo dye became more electrophilic and more favourable for dye reduction.

Evaluation of ethylenediamine-modified nanofibrillated cellulose/chitosan composites on adsorption of cationic and anionic dyes from aqueous solution

A multi-functional adsorbent was prepared by modifying nanofibrillated cellulose/chitosan composites with ethylenediamine (E-NFC/CS). The E-NFC/CS was characterized by FTIR and used for adsorption of cationic dye methylene blue (MB) and anionic dye new coccine (NC) from aqueous solution. The FTIR results showed that the E-NFC/CS contained more amino groups than the NFC/CS due to the modification for the NFC/CS with ethylenediamine. The results indicated that the maximum adsorption capacities occurred at pH 4.0 for MB and pH 2.0 for NC, respectively. The adsorption equilibrium time for MB and NC was 30 and 50min, respectively. In addition, the regenerated E-NFC/CS exhibited excellent adsorption performance for NC. It can keep almost 98% of the adsorption capacity after reused three times. Therefore, the E-NFC/CS can be potentially used as an effective adsorbent of cationic and anionic dyes in industrial effluents.

Solar Photocatalytic Mineralization of Dye New Coccine in Aqueous Phase Using Different Photocatalysts

The objective of this study was to examine the effect of band gap of photocatalyst on the decolorization of dye new coccine (NC). The concentration of NC in the present of CuO, Fe2O3, TiO2, and ZnO reduced to 50.5, 23.3, 0.1, and 0 mg L−1, respectively, after 5 h solar light irradiation. The concentration of NC in dark condition only decreased to 48.140, 45.079, 35.269, and 31.045 mg L−1 with CuO, Fe2O3, TiO2, and ZnO as photocatalysts, respectively, after 5 h contact time. The absorbance peaks and chemical oxygen demand (COD) concentration of NC in the presence of TiO2 and ZnO decreased to baseline and zero compared to the CuO and Fe2O3. The COD concentration of NC with CuO, Fe2O3, TiO2, and ZnO as photocatalysts reduced to 21, 13, 0, and 0 mg L−1, respectively, after 12 h of solar irradiation. The surface morphology of photocatalysts was examined by scanning electron microscope (SEM), and it was found that the particle size of CuO, Fe2O3, TiO2, and ZnO ranging 250–375, 250–600, 40–100, and 60–500 nm, respectively. In summary, the higher band gap energy level indicated greater photocatalytic degradation and mineralization of NC.

Adsorption characteristics of anionic azo dye onto large α-alumina beads

Adsorption of anionic azo dye, new coccine (NC), onto large α-alumina beads in aqueous media was systematically investigated as functions of pH and NaCl concentration. Adsorption amounts of NC decrease with increasing pH of solutions due to less positive charges of α-Al2O3 surface at high pH. At a fixed pH, the NC adsorption increases with decreasing NaCl concentration, indicating that NC molecules mainly adsorb onto α-Al2O3 by electrostatic attraction. Experimental results of NC adsorption isotherms onto α-Al2O3 at different pH, and ionic strength can be represented well by two-step adsorption model. The effects of NC on surface charge and surface modification of α-Al2O3 at the plateau adsorption are evaluated by streaming potential and Fourier transform infrared spectroscopy with attenuated total reflection technique (FTIR-ATR), respectively. On the basis of adsorption isotherms, surface charge effect, and surface modification, we suggested that the formation of a bridged bidentate complex between aluminum ions of α-Al2O3 and two oxygen atoms of a sulfonic group induced the adsorption of NC onto α-Al2O3.