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This paper presents low-cost and recyclable activated carbon (XLAC) derived from Xanthoceras sorbifolia Bunge hull for high-efficiency adsorption of Cd(II) and Hg(II) ions in industrial wastewater. XLAC was prepared through H3PO4 activation and was characterized using N2 adsorption-desorption, scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDX), and Fourier transform infrared (FTIR) spectroscopy. In single-metal-system adsorption experiments, the maximum adsorption capacities for Cd(II) and Hg(II) obtained under different experimental conditions were 388.7 and 235.6 mg·g−1, respectively. All adsorption equilibrium data fit perfectly with the Langmuir isotherm model. In a binary metal system, competitive studies demonstrated that the presence of Cd(II) significantly decreased the adsorption of Hg(II), but the adsorption of Cd(II) showed a little change in the presence of Hg(II). In addition, XLAC can be regenerated with a 0.01 mol·L−1 HNO3 solution and reused at least four times. The FTIR spectra revealed that a chemical interaction occurs between functional groups containing lone electron pairs in XLAC and metal ions. Overall, these results suggest that XLAC may be suitable as an adsorbent for heavy metal removal from wastewater streams. [ABSTRACT FROM AUTHOR]

A new and inexpensive lignocellulose/montmorillonite (LNC/MMT) nanocomposite was prepared by a chemical intercalation of LNC into MMT and was subsequently investigated as an adsorbent in batch systems for the adsorption-desorption of Ni(II) ions in an aqueous solution. The optimum conditions for the Ni(II) ion adsorption capacity of the LNC/MMT nanocomposite were studied in detail by varying parameters such as the initial Ni(II) concentration, the solution pH value, the adsorption temperature and time. The results indicated that the maximum adsorption capacity of Ni(II) reached 94.86 mg/g at an initial Ni(II) concentration of 0.0032 mol/L, a solution pH of 6.8, an adsorption temperature of 70°C, and adsorption time of 40 min. The represented adsorption kinetics model exhibited good agreement between the experimental data and the pseudo-second-order kinetic model. The Langmuir isotherm equation best fit the experimental data. The structure of the LNC/MMT nanocomposite was characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM), whereas the adsorption mechanism was discussed in combination with the results obtained from scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and Fourier-transform infrared spectroscopy analyses (FTIR). The desorption capacity of the LNC/MMT nanocomposite depended on parameters such as HNO3 concentration, desorption temperature, and desorption time. The satisfactory desorption capacity of 81.34 mg/g was obtained at a HNO3 concentration, desorption temperature, and desorption time of 0.2 mol/L, 60 ºC, and 30 min, respectively. The regeneration studies showed that the adsorption capacity of the LNC/MMT nanocomposite was consistent for five cycles without any appreciable loss in the batch process and confirmed that the LNC/MMT nanocomposite was reusable. The overall study revealed that the LNC/MMT nanocomposite functioned as an effective adsorbent in the detoxification of Ni(II)-contaminated wastewater. [ABSTRACT FROM AUTHOR]

Heavy metal wastewater treatment is a huge problem facing human beings, and the application degree of Salix psammophila resources produced by flat stubble is low. Therefore, it is very important to develop high-value products of Salix psammophila resources and apply them in the removal heavy metal from effluent. In this work, we extracted the cellulose from Salix psammophila, and cellulose nanofibers (CNFs) were prepared through TEMPO oxidation/ultrasound. The aerogel spheres derived from Salix psammophila (ASSP) were prepared with the hanging drop method. The experimental results showed that the Cu(II) adsorption capacity of the ASSP composite (267.64 mg/g) doped with TOCNF was significantly higher than that of pure cellulose aerogel spheres (52.75 mg/g). The presence of carboxyl and hydroxyl groups in ASSP enhanced the adsorption capacity of heavy metals. ASSP is an excellent heavy metal adsorbent, and its maximum adsorption values for Cu(II), Mn(II), and Zn(II) were found to be 272.69, 253.25, and 143.00 mg/g, respectively. The abandoned sand shrub resource of SP was used to adsorb heavy metals from effluent, which provides an important reference value for the development of forestry in this sandy area and will have a great application potential in the fields of the adsorption of heavy metals in soil and antibiotics in water. [ABSTRACT FROM AUTHOR]

Lignocellulose (LCE) was ultrasonically treated and intercalated into magnesium aluminum silicate (MOT) clay to prepare a nano-lignocellulose magnesium aluminum silicate polymer gel (nano-LCE-MOT) for the removal of Zn (II) from aqueous solution. The product was characterised using nitrogen adsorption/desorption isotherm measurements, Fourier-transform infrared spectroscopy, scanning electron microscopy and energy-dispersive X-ray spectroscopy. The conditions for the adsorption of Zn (II) on nano-LCE-MOT were screened, and adsorption kinetics and isotherm model analysis were carried out to explore the adsorption mechanism and achieve the optimal adsorption of Zn (II). Optimal adsorption was achieved at an initial Zn (II) concentration of 800 mg/L at 60 °C in 160 min at a pH of 4.52. The adsorption kinetics were explored using a pseudo-second-order model, with the isotherm adsorption equilibrium found to conform to the Langmuir model. The maximum adsorption capacity of the nano-LCE-MOT polymer gel toward Zn (II) is 513.48 mg/g. The materials with adsorbed Zn (II) were desorbed using different media, with HCl found to be the most ideal medium to desorb Zn (II). The optimal desorption of Zn (II) was achieved in 0.08 mol/L HCl solution at 65 °C in 60 min. Under these conditions, Zn (II) was almost completely desorbed from the adsorbents, with the adsorption effect after cycling being slightly different from that of the initial adsorption. [ABSTRACT FROM AUTHOR]