In this study, we develop a new composite material of Fe-Cu/D407 composite via using nanoscale zero-valent iron (nZVI) with copper deposited on chelating resin (D407) to remove nitrate from the water. The experimental results show that a remarkable nitrate removal and the selectivity of N₂ are 99.9% and 89.7%, respectively, under the anaerobic conditions of Cu/Fe molar ratio of 1:2, pH = 3.0. Even without of inert gas and adjusting the initial pH of the solution, the removal rate of nitrate by Fe-Cu/D407 reached to 85% and the selectivity of nitrogen reached to 55%. Meanwhile, the Fe-Cu/D407 maintained preferable removal efficiency of nitrate (100% - 92%) over a wide pH range of 3–11. In addition, the removal rate of the drinking water, lake water and wastewater from the Fe-Cu/D407 is still very high and the reactivity of Fe-Cu/D407 was relatively unaffected by the presence of dissolved ions in the waters tested. Moreover, the synergetic effect of Fe, Cu and D407 in the composite Fe-Cu/D407 were well investigated for the first time according to the analyses of TPR, XPS and EIS. The catalytic mechanism and denitrification routes were also proposed.

High performance activated carbon (HPAC) supported nanoscale zerovalent iron (nZVI) was prepared and used for recovery of silver. This composite material was characterized by Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and X-ray diffraction (XRD). The removal amount of Ag+ increased with pH values and temperature. The removal process achieved equilibrium within 40 min and the maximum removal capacity was 986.5 mg/g at 298 K. The composite material showed fast adsorption rate and high adsorption capacity because the presence of high surface area activated carbon could effectively inhibit aggregation of nanoscale zerovalent iron, thus enhancing its reactivity. The Ag+ removal followed pseudo-second-order kinetic model and Langmuir isotherm model. XPS and XRD characterizations were performed to elucidate removal mechanism. It could be concluded that both coordination adsorption and reductive precipitation contributed to removal of Ag+ on the nZVI/HPAC.

Thermal processing of materials is used in a very broad sense to cover all sets of technologies and processes for a wide range of industrial sectors and it refers to material development with a specific application potential due to its advantages over conventional synthesis methods. By applying hydrothermal technique, the development of advanced materials has been pursued, in order to retain heavy metals from wastewater. This research refers to nanosilica-based materials, specifically mesoporous silica, for which the heavy metal retention properties were improved by using nano-TiO₂ and nano-CeO₂, considering the properties of titanium and cerium. Advanced methods have been used to characterize the materials obtained as X-ray fluorescence (XRF) and energy-dispersive X-ray spectroscopy (EDS) for chemical composition; X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) for microstructural properties and BET analyser for pores and specific surface area characterization. The results showed higher retention efficiencies for the doped nanosilica.

The efficient removal of heavy metals from aqueous environment is imperative and challenging. A novel ternary composite constructed of diaminopyridine polymers, graphene oxide, and ferrite magnetic nanoparticles was designed by a facile in situ polymerization strategy for the removal of Pb(II) from aqueous solution. Detailed characterization of morphological, chemical, and magnetic properties was employed systematically to confirm the formation of the composite material. Batch adsorption experiment studies suggested that the composite was an excellent adsorbent for Pb(II) which was easily collected after use via exposure to an external magnetic field for 30 s. The effects of different parameters such as solution pH, adsorbent dosage, contact time, initial Pb(II) concentration, temperature, and co-existing ions were examined. The maximum adsorption capacity at pH = 5 was estimated to be 387.2 mg g⁻¹ at 298 K by the Langmuir isotherm model, accompanied by favorable adsorption recyclability according to the investigation of regeneration experiments. Thermodynamic studies revealed that the Pb(II) adsorption via our ternary composite was endothermic and spontaneous. The corresponding removal performance for effluent containing Pb(II) from the battery industry was successfully examined. The present results indicated that our designed adsorbent is beneficial to the practical Pb(II) removal in wastewater purification.

Robust and simple composite films for the removal of methyl orange (MO) and Cr(VI) have been prepared by combining chitosan, saponin, and bentonite at a specific ratio. There are several composite films (chitosan-saponin-bentonite (CSB)) prepared; among them, the composite films CSB₂:₃ and CSB₁:₁ have the highest removal efficiency toward MO and Cr(VI) where the maximum removal is 70.4% (pH 4.80) and 92.3% (pH 5.30), respectively. It was found that different types of adsorbate have different thermodynamic properties of the adsorption process; the adsorption of MO onto CSB₂:₃, chitosan, and acid-activated bentonite (AAB) proceeded endothermically, while the adsorption of Cr(VI) onto CSB₁:₁, chitosan, and AAB proceeded exothermically. The parameters of the adsorption were modeled by using isotherm and kinetic equations. The models of Langmuir, Freundlich, Redlich-Peterson, Sips, and Toth were used for fitting the adsorption isotherm data at a temperature of 30, 45, and 60 °C; all of the isotherm models could represent the data well. The result indicates that CSB₂:₃ has the highest adsorption capacity toward MO with qₘ of 360.90 mg g⁻¹ at 60 °C; meanwhile, CSB₁:₁ has the highest adsorption capacity toward Cr(VI) with qₘ 641.99 mg g⁻¹ at 30 °C. The pseudo-second-order model could represent the adsorption kinetics data better than the pseudo-first-order equation. The adsorption mechanism was proposed, and the thermodynamic properties of the adsorption were also studied.

Chitosan/Co-Fe-layered double hydroxides (CS/LDHs) were prepared by coprecipitation method, which is a kind of composite material with excellent properties. The structure of CS/LDHs was characterized by SEM, FTIR, and XRD, which proved that chitosan (CS) was successfully induced into hydrotalcite and CS/LDHs still possess the structural characteristics of hydrotalcite. The adsorption of 2,4-dichlorophenol (2,4-DCP) was studied with CS/LDHs and LDHs as adsorbent separately. The activity of immobilized laccase (L-CS/LDHs) with CS/LDHs as carrier is significantly better than that of the one (L-LDHs) using LDHs as carrier. Under the optimum conditions (pH = 6, 55 °C, 48 h), L-CS/LDHs exhibited better removal performance for 2,4-DCP (81.53%, 100 mg/L) than LDHs (63.55%); the removal of 2,4-DCP by L-CS/LDHs is excellent, exceeding 97% as its initial concentration below 60 mg/L. It includes the catalytic action of laccase and dechlorination of Fe³⁺ and Co²⁺, and the adsorption can be ignored under the optimal conditions. After 5 cycles, it maintained 67% (L-CS/LDHs) and 54% (L-LDHs) of the original removal.

In this paper, a crosslinked carboxymethyl starch (CCMS) was prepared with corn starch as the raw material, epichlorohydrin as the crosslinking agent, and chloroacetic acid as the etherifying agent through a series of crosslinking, alkalization, and etherification reactions, respectively. Nano-TiO₂ was loaded onto the surface of the CCMS by the sol-gel method to obtain a TiO₂/CCMS composite. The TiO₂/CCMS composite was characterized by XPS, XRD, SEM, and BET. XPS showed that the surface chemical composition of the TiO₂/CCMS composite material contained titanium; XRD diffraction patterns indicated that the crystal form of the TiO₂/CCMS composite was a combination of the CCMS and anatase TiO₂. The surface morphology obtained by SEM showed that there were nano-TiO₂ particles on the surface of the CCMS. The specific surface area of the TiO₂/CCMS composite was larger than that of CCMS. The adsorption-photodegradation performance of the TiO₂/CCMS composite was also studied under UV irradiation, and the results showed that significant adsorption-photodegradation synergies occurred.

In this paper, a magnetic nano-Fe₃O₄/triethanolamine/GO composite (TEA-GO-FE) was prepared by using graphene oxide (GO), triethanolamine (TEA), and ferric chloride. The result indicates that triethanolamine acted as an important role for the growing of Fe₃O₄ and adsorption ability of composite material. The synthesis mechanism of TEA-GO-FE was investigated through the medium of SEM-EDS, XRD, FT-IR, and TEM. The characterization results indicated Fe₃O₄ nanoparticles have been successfully loaded on the surface of graphene oxide and they were encapsulated by TEA and have excellent stability. According to the results of XRD, the general particle size of Fe₃O₄ on TEA-GO-FE was 27.5 nm. In order to understand the adsorption properties of TEA-GO-FE for Pb²⁺ and Cu²⁺, this article uses a static adsorption study method. The optimized adsorption conditions are as follows: pH = 5.0, temperature is 293.15 K, and the ion concentration is 100 mg/L. Under the optimized prerequisites, the adsorption capacities of Pb²⁺ and Cu²⁺ were 121.5 mg/g and 68.7 mg/g, separately. Through thermodynamic as well as kinetic studies, the adsorption process of Pb²⁺ and Cu²⁺ on TEA-GO-FE is a self-heating process.

Solid waste fly ash with low aluminum of Yunnan Province in China was used as pristine material to prepared chitosan-coated Na–X zeolite, and the obtained composite material was employed as As(V) adsorbent. Then, the prepared materials were characterized by XRD, FT-IR, and XPS. And the results suggested that the low aluminum fly ash was successfully convert into Na–X zeolite, and the mineralization between Si–OH of the obtained Na–X zeolite and C–OH of chitosan was the dominated mechanism for coated chitosan over the surface of Na–X zeolite. From the batch experiments of As(V) removal, it has been found that the coated chitosan could significantly improve As(V) performance of Na–X zeolite. The optimal working pH for removal As(V) by chitosan-coated Na–X zeolite was attained at pH 2.1 ± 0.1, and the maximum adsorption capacity was 63.23 mg/g. And the adsorption data at different interval time was excellent fitted by pseudo-second-order kinetic model. From the analyze of XPS, the results suggested that As(V) uptake over adsorbent by the bond of As–N and As–O and the surface hydroxyl group of Al–OH and –NH₂ were involved in uptake As(V) from acid wastewater.

The low-cost composite film was prepared by incorporating chitosan, berry soap fruit extract (rarasaponin), and bentonite as the raw materials. The produced chitosan/rarasaponin/bentonite (CRB) composite exhibits outstanding adsorption capability toward copper metal ions (Cu(II)). A series of static adsorption experiments were carried out to determine the isotherm and kinetic properties of CRB composite in the adsorption process. The adsorption equilibrium shows a good fit with the Langmuir isotherm model; the CRB composite has maximum uptake of Cu (II) of 412.70 mg/g; the kinetic adsorption data exhibit a good fit with the pseudo-second-order model. The thermodynamic parameters, ΔH°, ΔG°, and ΔS°, obtained from the isotherm data indicate that the uptake of copper ions by CRB composite is more favored at low temperatures. This study shows that physicochemical modified adsorbent, namely CRB composite, can remove Cu (II) better than pristine adsorbent of AAB and chitosan. The CRB composite also shows potential reusability.