ABSTRACT
A high-performance dye adsorbent of Mg/Al-layered double hydroxide modified water hyacinth hydrochar (MgAl@WH) was synthesized by a simple hydrothermal method. The surface functional groups, elemental composition, crystalline structure, and surface morphology of the prepared (MgAl@WH) were determined using different analytical techniques. The characterization results revealed that the (MgAl@WH) hydrochar surface offered more active adsorption sites, facilitating the mordant brown (anionic dye) adsorption, leading to its superior performance with much higher uptake capability (311.0 mg g-1 at 298 K) than Mg/Al double hydroxide nanosheets (MgAl DLHs, 80.2 mg g-1 at 298 K) and dried water hyacinth (WH, 10.0 mg g-1 at 298 K). The adsorption behavior of MgAL@WH follows the pseudo second order kinetic model (R2 = 0.999) and Langmuir isotherm model (R2 = 0.999). Moreover, MgAl@WH bonded efficiently with mordant brown dye via hydrogen bonding and interlayer anion exchange with monolayer formation. Additionally, the recycling tests revealed that the MgAl@WH can be reused over 10 cycles without significant change in the removal efficiency. Based on the obtained findings, Mg/Al-layered double hydroxide modified water hyacinth hydrochar (MgAl@WH), for its economic and environmental benefits, has recently been used as an efficient adsorbent to remediate industrial wastewater containing anionic dyes.
ABSTRACT
A novel chelating adsorbent, based on the functionalization of activated carbon (AC) derived from water hyacinth (WH) with melamine thiourea (MT) to form melamine thiourea-modified activated carbon (MT-MAC), is used for the effective removal of Hg2+, Pb2+, and Cd2+ from aqueous solution. Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and Brunauer-Emmett-Teller (BET) theory confirm the successful functionalization of AC with the melamine thiourea chelating ligand through the amidation reaction between the carboxyl groups of oxidized activated carbon (OAC) and the amino groups of melamine thiourea (MT) in the presence of dicyclohexylcarbodiimide (DCC) as a coupling agent. The prepared MT-MAC exhibited extensive potential for the adsorption of the toxic metal ions Hg2+, Pb2+, and Cd2+ from wastewater. The MT-MAC showed high capacities for the adsorption of Hg2+ (292.6 mg·g-1), Pb2+ (237.4 mg·g-1), and Cd2+ (97.9 mg·g-1) from aqueous solution. Additionally, 100% removal efficiency of Hg2+ at pH 5.5 was observed at very low initial concentrations (25-1000 ppb).The experimental sorption data could be fitted well with the Langmuir isotherm model, suggesting a monolayer adsorption behavior. The kinetic data of the chemisorption mechanism realized by the melamine thiourea groups grafted onto the activated carbon surface have a perfect match with the pseudo-second-order (PSO) kinetic model. In a mixed solution of metal ions containing 50 ppm of each ion, MT-MAC showed a removal of 97.0% Hg2+, 68% Pb2+, 45.0% Cd2+, 17.0% Cu2+, 7.0% Ni2+, and 5.0% Zn2+. Consequently, MT-MAC has exceptional selectivity for Hg2+ ions from the mixed metal ion solutions. The MT-MAC adsorbent showed high stability even after three adsorption-desorption cycles. According to the results obtained, the use of the MT-MAC adsorbent for the adsorption of Pb2+, Hg2+, and Cd2+ metal ions from polluted water is promising.
ABSTRACT
Here, a highly sensitive and selective copper ion (Cu2+) fluorescence sensor is reported. The Hematoporphyrin functionalized Graphene Oxide (HP-GO) fluorescence sensor were synthesized via esterification reaction between Graphene Oxide and Hematoporphyrin (HP). The HP-GO sensor was fully characterized by Fourier Transform Infrared Spectroscopy (FTIR), X-ray diffraction (XRD), Scanning Electrom Microscopy (SEM), UV-Vis spectroscopy, Transmission Electron Microscopy (TEM), Fluor meter spectroscopy, X-Ray photoelectron spectroscopy(XPS), and Raman spectroscopy measurements. The HP-GO sensor advertised two linear regions over the range of 0-1.18 × 103 nM and 3.93 × 103 to 47.27 nM of copper (II) with detection limit of 54 nM in the aqueous solution. The selectivity of HP-GO for Cu2+ is much higher than that of other metal ions due to the presence of aza macrocyclic ring on the surface of HP-GO which has a high binding affinity with Cu2+. Additionally, the HP-GO shows wide pH viable range (pH 6-10). The effect of other metal ions on the fluorescence intensity of the HP-GO was also studied and other metal ions show a low interference response in the detection of Cu2+. HP-GO sensor manifests advantages of high reproducibility (The quenched fluorescence of HP/GO-Cu can be recovered by EDTA), attractive long term fluorescence stability (>21 days) in water, also remarkable selectivity regarding number of metal ions (Na+, K+, Ca2+, Fe3+, Fe2+, Al3+, Pb2+, Mn2+, Mg2+, Co2+, Ni2+, Cr6+, Cd2+, Hg2+, and Zn2+), low toxicity and can detect Cu2+ in real water samples which acquire well for its promising in environmental applications.
ABSTRACT
A novel chelating adsorbent, based on the chemical modification of graphene oxide by functionalization amidinothiourea to form 2-imino-4-thiobiuret-partially reduced graphene oxide (IT-PRGO), is used for the effective extraction of the toxic metal ions Hg(II), Cu(II), Pb(II), Cr(VI), and As(V) from wastewater. FTIR and Raman spectroscopy, XRD, and XPS confirm the successful incorporation of the amidinothiourea groups within the partially reduced GO nanosheets through nucleophilic substitution reactions with the acyl chloride groups in the chemically modified GO. The IT-PRGO adsorbent shows exceptional selectivity for the extraction of Hg(II) with a capacity of 624 mg/g, placing it among the top of carbon-based materials known for the high capacity of Hg(II) removal from aqueous solutions. The maximum sorption capacities for As(V), Cu(II), Cr(VI), and Pb(II) are 19.0, 37.0, 63.0, and 101.5 mg/g, respectively. The IT-PRGO displays a 100% removal of Hg(II) at concentrations up to 100 ppm with 90%, 95%, and 100% removal within 15, 30, and 90 min, respectively, at 50 ppm concentration. In a mixture of six heavy metal ions containing 10 ppm of each ion, the IT-PRGO shows a removal of 3% Zn(II), 4% Ni(II), 9% Cd(II), 21% Cu(II), 63% Pb(II), and 100% Hg(II). A monolayer adsorption behavior is suggested based on the excellent agreement of the experimental sorption isotherms with the Langmuir model. The sorption kinetics can be fitted well to a pseudo-second-order kinetic model which suggests a chemisorption mechanism via the amidinothiourea groups grafted on the reduced graphene oxide nanosheets. Desorption studies demonstrate that the IT-PRGO is easily regenerated with the desorption of the metal ions Hg(II), Cu(II), Pb(II), Cr(VI), and As(V) reaching 96%, 100%, 100%, 96%, and 100%, respectively, from their maximum sorption capacities using different eluents. The IT-PRGO is proposed as a top performing remediation adsorbent for the extraction of heavy metals from waste and polluted water.
