Spectroscopic and statistical physics elucidation for Cu(II) remediation using magnetic bio adsorbent based on Fe3O4-chitosan-graphene oxide.

Efficient harnessing of heavy metal pollution is an urgent environmental task. Herein, magnetic bio adsorbent (MB) based on Fe3O4-chitosan-graphene oxide composite was fabricated via one step co-precipitation for adsorptive remediation of Cu(II). Remediation efficiency was evaluated by batch adsorption, meanwhile adsorption mechanism was elucidated by spectroscopic tests (XPS, UV-Vis absorption and fluorescent emission spectra), statistical physics formalism, isotherm and kinetic fittings. Results show, MB reaches adsorption percent and quantity of 87.61 % and 350.43 mg·g-1 for Cu(II) in 30 min. By virtue of paramagnetism, MB can be readily recovered with a permanent magnet for easy regeneration and cyclic use, thereby retaining adsorption quantity 279.99 mg·g-1 at the fifth cycle. The Freundlich and pseudo second order model satisfactorily describes the adsorption, designating chemical interaction as the rate limiting step. Statistical physics calculation suggests two points. (1) Multi-ionic adsorption mechanism with exothermic, spontaneous and energy lowering feature. (2) Density of adsorption sites increases with temperature, resulting in improved adsorption capacity. Spectroscopic analysis confirms the involvement of CO, CO, -NH2 in Cu(II) uptake via electron donation. These explorations contribute with novel theoretical illumination for understanding both the thermodynamic feature and atomic scale mechanism of common pollutants adsorption by bio adsorbent like Fe3O4-chitosan-graphene oxide.

Hydrochar as a bio-based adsorbent for heavy metals removal: A review of production processes, adsorption mechanisms, kinetic models, regeneration and reusability.

The spread of heavy metals throughout the ecosystem has extremely endangered human health, animals, plants, and natural resources. Hydrochar has emerged as a promising adsorbent for removal of heavy metals from water and wastewater. Hydrochar, obtained from hydrothermal carbonization of biomass, owns unique physical and chemical properties that are highly potent in capturing heavy metals via surface complexation, electrostatic interactions, and ion exchange mechanisms. This review focuses on removing heavy metals by hydrochar adsorbents from water bodies. The article discusses factors affecting the adsorption capacity of hydrochars, such as contact time, pH, initial metal concentration, temperature, and competing ions. Literature on optimization approaches such as surface modification, composite development, and hybrid systems are reviewed to enlighten mechanisms undertaking the efficiency of hydrochars in heavy metals removal from wastewater. The review also addresses challenges such as hydrochar regeneration and reusability, alongside potential issues related to its disposal and metal leaching. Integration with current water purification methods and the significance of ongoing research and initiatives promoting hydrochar-based technologies were also outlined. The article concludes that combining hydrochar with modern technologies such as nanotechnology and advanced oxidation techniques holds promise for improving heavy metal remediation. Overall, this comprehensive analysis provides valuable insights to guide future studies and foster the development of effective, affordable, and environmentally friendly heavy metal removal technologies to ensure the attainment of safer drinking water for communities worldwide.

Turn Waste Golden Tide into Treasure: Bio-Adsorbent Synthesis for CO2 Capture with K2FeO4 as Catalytic Oxidative Activator.

Converting Sargassum horneri (SH)-a harmful marine stranding that can cause golden tide-to highly porous bio-adsorbent material (via one-step catalytic oxidative pyrolysis with K2FeO4) can be a strategically useful method for obtaining low-cost materials suitable for CO2 capture. In this manuscript, the behavior of different mass ratios of K2FeO4/SH precursor acting on the surface physicochemical properties of carbon materials are reported. The results suggest that specific surface area and total pore volume first increased to the mass ratio of K2FeO4/carbon precursor, then decreased. Among the samples prepared, the highest specific surface area was obtained with a K2FeO4/SH precursor ratio of 1:4 (25%-ASHC), and the CO2 adsorption performance was significantly increased and faster compared with the original biochar. The fitted values of the three kinetic models showed that the double exponential model provided the best description of carbon adsorption, indicating both physical and chemical adsorption; 25%-ASHC also exhibited excellent cyclic stability. The improved CO2 adsorption performance observed after K2FeO4 activation is mainly due to the increase in material porosity, specific surface area, and the enrichment of nitrogen and oxygen functional groups.

Unraveling the mechanism of iodate adsorption by anthocyanin-rich fruit waste as green adsorbents for Applications of radioactive iodine remediation in water environment.

In aquatic settings, radioactive iodine from nuclear waste can exist as iodate (IO3-). This study explored the efficiency and mechanism of IO3- adsorption by minimally modified anthocyanin-based adsorbents. Pomegranate peels and mangosteen pericarps were selected from an initial screening test and could remove over 70% of 10 mg/L IO3-. The adsorbents yielded adsorption capacity (q) of 9.59 mg/g and 2.31 mg/g, respectively, at room temperature. At 5 °C, q values increased to 14.5 and 5.13 mg/g, respectively. Pomegranate peels showed superior performance, with approximately 4 times the anthocyanin content of mangosteen pericarps. Both adsorbents took 120 min to reach adsorption equilibrium, and no desorption was observed after 8 days (I-131 half-time). Confirmation of physisorption was indicated by the fit of the pseudo-first-order reaction model, negative entropy (exothermic), and negative activation energy (Arrhenius equation). IO3- inclusion was confirmed through adsorbent surface modifications in scanning electron microscope images, the increased iodine content post-adsorption in energy-dispersive X-ray spectroscopy analysis, and alterations in peaks corresponding to anthocyanin-related functional groups in Fourier transform infrared spectroscopy analysis. X-ray absorption near-edge spectroscopy at 4564.54 eV showed that iodine was retained in the form of IO3-. Through the computational analysis, electrostatic forces, hydrogen bonds, and π-halogen interactions were deduced as mechanisms of IO3- adsorption by anthocyanin-based adsorbents. Anthocyanin-rich fruit wastes emerged as sustainable materials for eliminating IO3- from water.

Recovering and potentially applying of alginate like extracellular polymers from anaerobic digested sludge.

Extracellular polymeric substances (EPS) are biopolymers contained in both aerobic and anaerobic sludge. In EPS, alginate like extracellular polymers (ALE) is thought as a highly valued material, which have been widely studied with aerobic sludge. Nevertheless, a curiosity on ALE remains in anaerobic digested sludge (ADS). With 5 different sludge sources, anaerobic digestion of excess sludge was conducted in a batch mode, and then ADS was used to extract ALE and to analyze its physicochemical properties for potential applications. The yield of ALE extracted from ADS (ALE-ADS) ranged from 119.4 to 179.4 mg/g VSS. The compositional characteristics of ALE-ADS observed by FT-IR, 3D-EEM and UV-Vis spectroscopy revealed that there were minor differences in the composition and property of ALE-ADS but a similarity of 62 %-70 % to a commercial alginate remained in terms of chemical functional groups. Moreover, ALE-ADS composed of 1,4-linked ß-d-mannuronic acid (M) and 1,4 α-l-guluronic acid (G) residues that form blocks of GG (20.8 %-33.8 %), MG (12.8 %-30.1 %) and MM (6.6 %-15.1 %), respectively. Based on the gel-forming capacity, film-forming property, adsorbility, and amphiphilicity, ALE-ADS seems potential as a water-proof coating with even a better performance than the commercial alginate, as a seed coating with an increased germination rate, and as a bio-adsorbent with a similar performance to the commercial alginate and ALE from aerobic sludge.

Preparation of a new gel-type lignin-based cationic adsorption resin for efficient removal of Ca2+ from aqueous solutions.

Presently, most studies on modified lignin focused on the adsorption to heavy metal cations, but rarely to Ca2+ in hard water. Therefore, this work prepared a new gel-type lignin-based cationic adsorption resin (E-LSAF) through the crosslinking and curing of alkali lignin grafted by sodium sulfite sulfonated acetone to remove Ca2+ in water. Under the determined optimum synthesis conditions, E-LSAF with a highest sulfonic group content of 1.99 mmol/g was obtained. Structural and physicochemical measuring results showed E-LSAF was a gel-type resin, owning strong hydrophilicity, high mechanical strength, excellent thermal stability and acid-alkaline resistance. Adsorption results indicated the adsorption of E-LSAF to Ca2+ was well-fitted by Langmuir model, and the maximum adsorption capacity reached 45.8 mg/g. Pseudo-second-order model can describe this adsorption process well, suggesting it a chemisorption process. Dynamic column adsorption results showed E-LSAF could transform hard water into soft or even very soft water. The regeneration efficiency still maintained 80 % after 5 cycles. The adsorption mechanism was attributed to electrostatic attraction, ion exchange and complexation. This work provided a high-performance lignin-based cationic adsorption material with high adsorption capacity to Ca2+ and excellent acid-alkaline resistance, which filled the research gap of using modified sulfonated lignin to remove Ca2+ from water.

Efficient and Selective Removal of Organic Cationic Dyes by Peel of Brassica juncea Coss. var. gemmifera Lee et Lin-Based Biochar.

The design and preparation of cheaper, greener and more efficient adsorbents is essential for the removal of pollutants by adsorption. In this study, biochar was prepared from peel of Brassica juncea var. gemmifera Lee et Lin (PoBJ) using a facile, low-temperature and vacuum pyrolysis, and the adsorption mechanism toward organic dyes in aqueous solution was elucidated. The adsorbent was characterized by XPS, FT-IR and SEM, and zeta potential techniques. The adsorption ability of PoBJ biochar for cationic dyes (methylene blue, brilliant green, calcein-safranine, azure I, rhodamine B), anionic dyes (alizarin yellow R), and neutral dyes (neutral red) revealed that the biochar exhibited adsorption selectivity toward cationic dyes. The effects of different factors on the adsorption performance of PoBJ biochar, as well as the adsorption kinetics and thermodynamics, were further investigated by using methylene blue as the model adsorbate. These factors included temperature, pH, contact time and dye concentration. The experimental results showed that BJ280 and BJ160 (prepared at 280 °C and 160 °C, respectively) possessed relatively higher adsorption capacity of 192.8 and 167.40 mg g-1 for methylene blue (MB), respectively, demonstrating the possibility of utilization of PoBJ biochar as a superior bio-adsorbent. The experimental data of BJ160 toward MB were correlated with various kinetic and isothermal models. The results indicated that the adsorption process was consistent with the Langmuir isotherm model and nonlinear pseudo-second-order kinetic model. Thermodynamic parameters indicated that the adsorption of MB onto BJ160 was exothermic. Thus, the low-temperature prepared PoBJ biochar was an environmentally friendly, economic and efficient cationic dye adsorbent.

Preparation of manganese-oxides-coated magnetic microcrystalline cellulose via KMnO4 modification: Improving the counts of the acid groups and adsorption efficiency for Pb(II).

Herein, the manganese-oxides-coated magnetic microcrystalline cellulose (MnOx@Fe3O4@MCC) was prepared by coprecipitation and subsequently modified with KMnO4 solution at room temperature, which was in turn applied for the removal of Pb(II) from wastewater. The adsorption properties of Pb(II) on MnOx@Fe3O4@MCC were investigated. The kinetics and isothermal data of Pb(II) were described well by the Pseudo-second-order model and the Langmuir isotherm model, respectively. At pH = 5, 318 K, the Langmuir maximum Pb(II) adsorption capacity of MnOx@Fe3O4@MCC was 446.43 mg/g, which is higher than many documented bio-based adsorbents. The results of Fourier transform infra-red and X-ray photoelectron spectroscopy indicated that the adsorption mechanisms for Pb(II) mainly involved surface complexation, ion exchange, electrostatic interaction and precipitation. Interestingly, the increased amount of carboxyl group on the surface of microcrystalline cellulose modified by KMnO4 was one of the important reasons for the high Pb(II) adsorption performance of MnOx@Fe3O4@MCC. Furthermore, MnOx@Fe3O4@MCC exhibited excellent activity (70.6 %) after five consecutive regeneration cycles, indicating its high stability and reusability. Endorsing to the cost-effectiveness, environmentally friendliness, and reusable nature, MnOx@Fe3O4@MCC can be counted as a great alternative contender for the remediation of Pb(II) from industrial wastewater.

Graphene oxide incorporated chitosan/acrylamide/itaconic acid semi-interpenetrating network hydrogel bio-adsorbents for highly efficient and selective removal of cationic dyes.

In recent years, polymeric bio-adsorbents offers high removal efficiency, superior adsorption capacity and selectivity against various pollutants in aqueous medium. While designing these adsorbents, their environmental friendliness, sustainability, renewability, easy accessibility, and cost-effectiveness should be considered. In this study, GO incorporated semi-interpenetrating network (semi-IPN) nanocomposite hydrogels (CS/AAm/IA/GO) were obtained by free radical copolymerization of acrylamide (AAm) and itaconic acid (IA) in the presence of chitosan (CS) as an environmentally friendly bio-adsorbent. GO significantly improved the thermal stability, compressive strength, and percentage swelling of the hydrogel. The selective adsorption studies demonstrated that methylene blue (MB) was the most efficiently removed dye from both individual and mixed dye systems with 99.8 % removal efficiency. The adsorption capacity was found to be 247.47 mg g-1 using 0.025 g hydrogel adsorbent containing 0.5 wt% of GO and an initial MB concentration of 5 mg L-1 at pH 8 over 90 min at room temperature. The kinetic and isotherm studies revealed that the adsorption process followed the pseudo-second-order kinetic model and Langmuir adsorption isotherm. Thermodynamic studies suggested the spontaneous and endothermic nature of MB adsorption. Also, the MB removal efficiency above 96 % was obtained after 7 consecutive adsorption-desorption cycles while maintaining the structural stability of the bio-adsorbent.

Fast-growing cyanobacteria bio-embedded into bacterial cellulose for toxic metal bioremediation.

Cyanobacterial biomass and cellulose-based materials have been used separately as green bio-adsorbents for the removal of toxic metals from water. Hybrid materials made of living microbial cells encased in a solid matrix have shown good potential for bioremediation. Here, the fast-growing cyanobacterium Synechococcus elongatus UTEX 2973 was embedded in situ into bacterial cellulose (BC), a robust biopolymer rich in hydroxyl groups with excellent water holding capacity. The living material was obtained by injecting S. elongatus into a Komagataeibacter sucrofermentans culture producing BC. Several types of BC/S. elongatus (BC/SE) materials were developed including small spheroids and flat films with different cyanobacteria loads via simple adjustments of the biosynthesis process parameters. BC/SE spheroids were evaluated for toxic copper removal and exhibited excellent adsorption properties compared to pure BC with a maximum capacity of 156.25 mg g-1. Thus, this simple bio-embedding approach holds promises in the development of living materials for environmental applications.

Adsorption of methyl violet dye onto a prepared bio-adsorbent from date seeds: isotherm, kinetics, and thermodynamic studies.

Raw date seeds, as prospective natural, broadly obtainable and low-price agricultural waste for adsorbing cationic dyes from aqueous solutions, have been studied. In this work, Iraqi date seeds were prepared and characterised using X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy and Brunauer-Emmett-Teller (BET) surface area analysis before being used as an efficient bio-adsorbent for methyl violet (MV) dye removal. Adsorption tests were conducted with three investigated parameters, namely, time of contact, first adsorbate concentration and adsorbent dose. Compared with the pseudo first-order model (coefficient of determination = 0.9001), the pseudo second-order model was determined to be the best-fitting model with a coefficient of determination (R2) of 0.9917. The equilibrium isotherms for MV were obtained, and their ultimate capacity of adsorption was (59.5 mg g1). Two isotherm models, Langmuir and Freundlich, were studied to fit the equilibrium data. Compared with the Freundlich isotherm model (R2 = 0.8154), the Langmuir model functioned better as an adsorption isotherm with R2 of 0.9837. In addition, the adsorption process was endothermic and spontaneous. The date seeds acted as active adsorbents to remove MV from the aqueous solutions in the model experiments.

Cellulose-based bio-adsorbent from TEMPO-oxidized natural loofah for effective removal of Pb(II) and methylene blue.

Excessive discharge of inorganic and organic contaminants in water poses a serious threat to the ecosystems. However, most synthetic adsorbents lack cost-effectiveness in terms of preparation. Interestingly, loofah sponge (LS) was a natural absorbent that could effectively remove pollutions in wastewater, but its adsorption capacity is barely satisfactory. Herein, we present a novel strategy of TEMPO-oxidized loofah sponge (TOLS) to boost the adsorption performance of LS. The batch experiments demonstrated that the maximum removal capacity of TOLS for Pb(II) and methylene blue (MB) was 96.6 mg/g and 10.0 mg/g, respectively, which were 3.5 and 1.3 times that of pristine LS. Notably, the continuous-flow reaction testing of the mixed solution revealed that the elimination rate of Pb(II) and MB was still better than 90 % even after 16 h. Such excellent performance was benefit from the enhanced specific surface area and surface carboxyl content of TOLS. This work offers new insights into the rational development of multifunctional and inexpensive cellulose-based bio-adsorbents for wastewater remediation.

Adsorption and removal of crystal violet dye from aqueous solution by modified rice husk.

An approach to removing crystal violet (CV) dye from aqueous solutions was investigated by introducing a xanthate group on charred rice husk. The newly prepared charred rice husk (CRH) and xanthated rice husk (XRH) were characterized by XRD, SEM, FTIR, and elemental analysis. A batch technique was used to adsorb CV dye in aqueous suspensions. Different adsorbent quantities, concentrations, pH, and contact times were investigated to find the effect of these parameters. The optimum pH for both CRH and XRH was found to be 10. The adsorption capacity of CV dye onto CRH and XRH was found to be 62.85 mg/g and 90.02 mg/g at pH10, respectively. Langmuir isotherms could be reasonably explained by the experimental data. Within 60 min, equilibrium was achieved. Similarly, the kinetic data are best suited to the pseudo-second-order model. In comparison to XRH with CRH, XRH was found more efficient and can be used as a feasible alternative for removing CV dye from aqueous solutions.

Enhanced removal of Eriochrome Black T from water using biochar/layered double hydroxide/chitosan hybrid composite: Performance evaluation and optimization using BBD-RSM approach.

In this research work, a novel hybrid composite consisting of biochar (B), layered double hydroxide (CuFe) and chitosan (CS) (B-CuFe-CS) was produced using an ultrasonication-assisted co-precipitation method. The resultant composite was employed for adsorptive removal of Eriochrome black T (EBT) from water. Physicochemical characterization indicated that the B-CuFe-CS containing 10 wt % CS exhibited a heterogeneous structure with better crystallographic and textural characteristics. The B-CuFe-CS with abundant surface functionalities (-CO, -C-O, -OH, -NO3, and MMO), facilitates faster and enhanced removal of the EBT. The kinetic results showed better fitting to the pseudo-second order model, and equilibrium was achieved within 30 min. Equilibrium data was well explained by Langmuir and Redlich Peterson isotherm models (R2 > 0.98), indicating the EBT removal onto B-CuFe-CS followed monolayer adsorption. The maximum adsorption capacity was 806.4 mg/g, which was higher than pristine B-CuFe (476.19 mg/g) and many other adsorbents. The spectroscopic analysis (FTIR and XPS) and experimental results suggested that EBT adsorption is mainly governed by electrostatic, chemical and anion-exchange interactions. It is evident from these results that coupling B-CuFe composite with bio-filler (chitosan) resulted in an efficient bio-adsorbent to effectively purify dye-contaminated water streams.

Waste biomass based potential bioadsorbent for lead removal from simulated wastewater.

Present study deals with the lead removal from simulated wastewater using cost effective bio-adsorbent of mango seeds cover with kernel (M), and jamun seeds cover with kernel (JP). Lead removal optimization of adsorption parameters has been analyzed by using Response surface methodology (RSM). The optimum adsorption was attained at speed of 500 rpm, 60 mg, pH 6.5 and contact time of 120 min. The adsorption capacities are around 39.15 mg/g of M and 20.28 mg/g of JP bio-adsorbent, and also the maximum Pb removal were observed Ì´ 94.85% and 92.78%, respectively. The regression coefficient was best fitted for both bio-adsorbents are Freundlich model and pseudo-first order reaction kinetic.

Waste seeds of Mangifera indica, Artocarpus heterophyllus, and Schizizium commune as biochar for heavy metal removal from simulated wastewater.

The threat of arsenic contamination in water is a challenging issue worldwide. Millions of people utilize untreated groundwater having high levels of arsenic in developing countries. Design Expert 6.0.8 has been used to design experiments and carried out statistical analysis for optimization of different parameters. It is of prime importance to develop cheap environment friendly bio-sorbent for protecting health of the poor from ill effects of arsenic. In the present investigation, we prepared bio-sorbent from the solid waste seed biomass of Mangifera indica (M), Artocarpus heterophyllus (JF), and Schizizium commune (JP). The characterization of bio-sorbents has been done by using different techniques namely FTIR and XRD. Arsenic concentration was estimated using ICP and adsorption parameters optimized for pH, adsorbent dose, and initial arsenic concentration. At pH 8.4, kinetics study of arsenic removal was M (94%), JF (93%), and JP (92%) for initial concentration of 2.5 ppm. The adsorption kinetics was well explained by Freundlich model and pseudo-second reaction order. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13399-021-02078-5.

Fabrications and applications of hemicellulose-based bio-adsorbents.

Super adsorbents exhibit great potential to remove pollutants from media or store considerable amounts of water, which may undermine the pressure triggered by environmental pollution and shortage of water resources. Super adsorbents made from biopolymers have been an attractive topic because of biodegradability, renewability and outstanding adsorption capacity. Hemicelluloses are a type of biopolymers very abundant in agricultural, forestry and pulping industrial wastes. Hemicellulose-based bio-adsorbents are thriving because the inherent chemical structures and physical properties of hemicelluloses make themselves easy to be processed into matrix materials applicable in super adsorbents. This review summarizes recent studies in hemicellulose-based bio-adsorbents, i.e. hydrogels and activated carbons, from the perspectives of types, applications, fabrication methods, the elements affecting the adsorption performance and the kinetics of adsorption process, which thus helps to further improve the properties of hemicellulose-based bio-adsorbents and to promote the industrial production and utilization of hemicelluloses and hemicellulose-based bio-adsorbents.

Fabrication of novel bio-adsorbent and its application for the removal of Cu(II) from aqueous solution.

As eco-friendly adsorption material, hydroxyapatite (Ca5(PO4)3OH, HA) has been extensively applied to the removal of heavy metal ions. However, separating and recovering of HA powder after the adsorption process limits their application. Alginate-based composite beads (HCA) encapsulated with HA and cellulose were designed to remove Cu(II) from aqueous solution. Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS) were used for characteristic analysis. An extensive discussion in terms of HCA adsorption capacity, effect of various Cu(II) concentration, and analysis of the involved mechanisms of Cu(II) removal on the biosorption. HCA beads showed that the maximum adsorption capacity for Cu(II) of 64.14 mg/g at pH = 5 with 8 h contact time. The Langmuir adsorption isotherm and second-order kinetic model gave the closest fit. HCA beads display good regeneration ability after four cycles and offer potentiality for practical application.

Two Fascinating Polysaccharides: Chitosan and Starch. Some Prominent Characterizations for Applying as Eco-Friendly Food Packaging and Pollutant Remover in Aqueous Medium. Progress in Recent Years: A Review.

The call to use biodegradable, eco-friendly materials is urgent. The use of biopolymers as a replacement for the classic petroleum-based materials is increasing. Chitosan and starch have been widely studied with this purpose: to be part of this replacement. The importance of proper physical characterization of these biopolymers is essential for the intended application. This review focuses on characterizations of chitosan and starch, approximately from 2017 to date, in one of their most-used applications: food packaging for chitosan and as an adsorbent agent of pollutants in aqueous medium for starch.

Preparation of TiO2/cellulose nanocomposites as antibacterial bio-adsorbents for effective phosphate removal from aqueous medium.

The design of environmentally benign bio-adsorbents for the removal of phosphate from aqueous medium was an economic and effective way for controlling eutrophication. Herein, we prepared three kinds of TiO2/cellulose (CE-Ti) nanocomposites by a facile hydrolysis-precipitation method, and used them as antibacterial bio-adsorbents for the removal of phosphate from aqueous medium. Multiple techniques including Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) and thermogravimetric analysis (TGA) were employed to characterize the nanostructure and characteristics of the prepared CE-Ti nanocomposite. The adsorption capacity of the CE-Ti was 19.57 mg P g-1 according to the Langmuir model, which was 6 times higher than that of CE. Importantly, the bacterial inhibition zone of the CE-Ti was 2.88 mm (that of CE was 0 mm), indicating that CE-Ti had good antibacterial activity that could reduce the attachment of the microorganism to the surface of CE-Ti, which was suitable for long-term phosphate removal. Moreover, the CE-Ti had good adsorption selectivity and anti-interference capability, according to interfering ions and ion strength experiments. Furthermore, Ti4+ leakage tests suggested that CE-Ti was highly stable under acidic, neutral and alkali conditions. These results indicated that the CE-Ti nanocomposite could be utilized as a promising antibacterial bio-adsorbent for effective phosphate removal from aqueous medium.