Layered by layered construction of three novel ZnCo-LDHs/g-C3N4 for the removal of sunset yellow by adsorption-photocatalytic process.

The removal of organic dyes has attracted attention by adsorption-photocatalytic synergetic process in water treatment technology. Three novel ZnCo-LDHs/g-C3N4 were successfully prepared for the first time by layered construction technique through the hydrolysis of triethanolamine in this paper. They exhibited high specific surface area which facilitates the adsorption of sunset yellow (SY) from solution to catalyst surface. All the target pollutant dyes are very effectively removed by the three ZnCo-LDHs/g-C3N4 composites through synergetic effect of adsorption and photocatalysis process under UV irradiation (λ = 365 nm). The order of synergistic degradation effect for SY is as follows: ZnCo-LDHs/g-C3N4-3 (99.6%) > ZnCo-LDHs/g-C3N4-2 (99.5%) > ZnCo-LDHs/g-C3N4-1 (99.3%) > pure g-C3N4 (77.4%) > pure ZnCo-LDHs (44.2.6%) at the initial concentration of 75 mg L-1. ZnCo-LDHs/g-C3N4-3 has the largest k value (0.0284 min-1) in SY degradation, which is 2.8 times that of g-C3N4. ZnCo-LDHs/g-C3N4-3 is a very promising adsorption-photocatalyst for the removal of SY from wastewater. The electron spin resonance experiments demonstrate that OH·, 1O2, and O2- are the dominant active species and oxides SY together. This result demonstrates that the three ZnCo-LDHs/g-C3N4 have practical applications as efficient adsorption-photocatalytic materials and also provides a synergetic strategy for the removal of SY wastewater.

Rational construction and understanding the effect of metal cation substitution of three novel ternary Zn-Co-Ni-LDHs from 2D to 3D and its enhanced adsorption properties for MO.

The layered double hydroxides (LDHs) have attracted attention in the water treatment field. In this paper, three novel ternary Zn-Co-Ni-LDH adsorbents were prepared successfully through rational construction from 2D to 3D using triethanolamine (TEA) as an alkali source and a structural controlling reagent by hydrothermal technique. Samples were characterized by the SEM, XRD, XPS, FTIR, BET, solid-state UV/vis spectra, and TG. Three Zn-Co-Ni-LDHs exhibited higher crystallinity and surface area which were beneficial to the adsorption for methyl orange (MO). The maximum adsorption capacity of three Zn-Co-Ni-LDH adsorbents can even reach as high as 1871.65 mg·g-1, 1799.56 mg·g-1, and 1646.44 mg·g-1 for MO, respectively, which surpass those of most previously reported LDH-based adsorbents. The pseudo-second-order kinetic equation fitted the kinetic data of adsorption, while the equilibrium adsorption isotherm data followed the Langmuir model. The adsorption mechanism, electrochemical, and the antibacterial properties of three Zn-Co-Ni-LDHs were also discussed. This results not only demonstrates that three Zn-Co-Ni-LDHs are practical interest as an efficient adsorbent for the removal of MO from dye waste water, but also provides a strategy for the rational design through three ternary Zn-Co-Ni-LDHs from 2D to 3D.