Char as a carbon-rich material, can be produced under pyrolytic conditions, wildfires or prescribed burn offs for fire management. The objective of this study was to elucidate mechanistic interactions of copper (Cu2+) and nickel (Ni2+) with different chars produced by pyrolysis (green waste, GW; blue-Mallee, BM) and forest fires (fresh-burnt by prescribed fire, FC; aged char produced by wild fire, AC). The pyrolytic chars were more effective sorbents of Cu2+ (∼11 times) and Ni2+ (∼5 times) compared with the forest fire chars. Both cross-polarization (CPMAS-NMR) and Bloch decay (BDMAS-NMR) 13C NMR spectroscopies showed that forest fire chars have higher woody components (aromatic functional groups) and lower polar groups (e.g. O-alkyl C) compared with the pyrolytic chars. The polarity index was greater in the pyrolytic chars (0.99–1.34) than in the fire-generated chars (0.98–1.15), while aromaticity was lower in the former than in the latter. Fourier transform infrared (FTIR) and Raman spectroscopies indicated the binding of carbonate and phosphate with both Cu2+ and Ni2+ in all chars, but with a greater extent in pyrolytic than forest fire-generated chars. These findings have demonstrated the key role of char's oxygen-containing functional groups in determining their sorption capacity for the Cu2+ and Ni2+ in contaminated lands.

Clay minerals are the most popular adsorbents/amendments for immobilizing heavy metals in contaminated soils, but the dissolved organic matter (DOM) in soil environment would potentially affect the adsorption/immobilization capacity of clay minerals for heavy metals. In this study, the effects of DOM derived from chicken manure (CM) on the adsorption of cadmium (Cd2+) on two clay minerals, bentonite and zeolite, were investigated. The equilibrium data for Cd2+ sorption in the absence or presence of CM-DOM could be well-fitted to the Langmuir equation (R2 > 0.97). The presence of CM-DOM in the aqueous solution was found to greatly reduce the adsorption capacity of both minerals for Cd2+, in particular zeolite, and the percentage decreases for Cd2+ sorption increased with increasing concentrations of Cd2+ as well as CM-DOM in aqueous solutions. The adsorption of CM-DOM on zeolite was greater than that on bentonite in the absence of Cd2+, however, a sharp increase was observed for CM-DOM sorption on bentonite with increasing Cd2+ concentrations but little change for that on zeolite, which can be attributed to the different ternary structures on mineral surface. The CM-DOM modified clay minerals were utilized to investigate the effect of mineral-adsorbed CM-DOM on Cd2+ sorption. The adsorbed form was found to inhibit Cd2+ sorption, and further calculation suggested it primarily responsible for the overall decrease in Cd2+ sorption on clay minerals in the presence of CM-DOM in aqueous solutions. An investigation for the mineral surface morphology suggested that the mineral-adsorbed CM-DOM decreased Cd2+ sorption on bentonite mainly through barrier effect, while in the case of zeolite, it was the combination of active sites occupation and barrier effect. These results can serve as a guide for evaluating the performance of clay minerals in immobilizing heavy metals when animal manure is present in contaminated soils.

The exposures of pharmaceutical antibiotics in water solution caused potential risks for ecological environment and human health. In the present study, porous covalent triazine frameworks (CTFs) were synthesized and the adsorption behavior of sulfamethoxazole (SMX) and tylosin (TL) was investigated. The CTFs were characterized by X-ray diffraction, transform infrared and N2 adsorption/desorption. Sulfamethoxazole displayed much stronger adsorption than tylosin on microporous CTF-1 adsorbent due to the pore-filling effect. While the adsorption of bulky tylosin on microporous CTF-1 was suppressed because of the size exclusion effect. Additionally, the porous CTFDCBP showed stronger adsorption affinity and faster adsorption kinetics than other porous adsorbents, which was attributed to wide pore size distribution and open pore structure. Findings in this study highlight the potential of using porous CTFs as a potential adsorbent to eliminate antibiotics from water, especially for selective adsorption of bulky molecular pollutant.

With the extensive application of graphene oxide (GO), it is noticeable that part of GO is directly/indirectly released into the environment and widespread research indicated that it had adverse influences on human health and ecological balance. In this work, a novel nanobelt-like Ca/Al layered double hydroxides (CA-LDH) was synthesized and applied as efficient coagulant for the removal of GO from aqueous solutions. The results indicated that neutral pH, co-existing cations and higher temperature were beneficial to the coagulation of GO. The sequence of cation effect for promoting of GO coagulation was Ca2+ > Mg2+ > K+ > Na+, whereas the effect of anions on GO coagulation was PO43− > CO32− > SO42− > Cl−. Comparing with anions, the cations showed more dominate effect for GO coagulation than anions. Hydrogen bonds and electrostatic interaction were the main coagulation mechanisms for GO coagulation, which were evidenced by FT-IR and XPS analysis. Specifically, for the first time, the reclaimed product of CA-LDH after GO coagulation (CA-LDH + GO) was applied as adsorbents for the secondary application in the removal of heavy metal ions from aqueous solutions. Interestingly, the CA-LDH + GO still had high adsorption capacities, i.e., the maximum adsorption capacities (qmax) for Cu(II), Pb(II), and Cr(VI) were 122.7 mg/g, 221.2 mg/g and 64.4 mg/g, respectively, higher than other similar materials. This paper highlighted the LDH-based nanomaterials are promising materials for the elimination of environmental pollutants and the migration and transformation of carbon nanomaterials in the natural environment.

Three novel organic vermiculites (VER) modified by amphoteric surfactants (BS, SB and PBS) with different negatively charged groups (carboxylate, sulfonate and phosphate) were demonstrated and used for removal of bisphenol A (BPA) and tetrabromobisphenol A (TBBPA). The difference in the structure and surface properties of modified vermiculites were investigated using a series of characterization methods. BS and SB surfactant mainly adsorbed on the surface and hard to intercalate into the interlayer of VER, while both adsorption and intercalation occurred in PBS modification. This difference resulted in different packing density of surfactant and hydrophobicity according to the results of contact angle, and affect the adsorption capacities ultimately. The adsorption of two pollutants onto these modified vermiculites were very fast and well fitted with pseudo-second-order kinetic model and Langmuir isotherm. PBS-VER exhibited the highest adsorption capacity (92.67 and 88.87 mg g−1 for BPA and TBBPA, respectively) than other two modified vermiculites in this order PBS-VER > BS-VER > SB-VER. The ionic strength (Na+, Ca2+) and coexisting compounds (Pb2+, humic acid) have different effects on the adsorption. PBS-VER had a good reusability and could remove ionic (methylene blue and orange G) and molecular (BPA) pollutants simultaneously and effectively due to the function of amphoteric hydrophilic groups and alkyl chains. The results might provide novel information for developing low-cost and effective adsorbents for removal of neutral and charged organic pollutants.

Samplers made with different materials were tested for the quantitative collection and recovery of mercury halides from the atmospheric air. The tested adsorbent materials included zirconia (ZrO2), titania (TiO2), melted SiO2 (quartz wool) and potassium chloride (KCl). Different processes affecting the sampler efficiency were investigated specifically: breakthrough during sampling because of the surface passivation and loss of already collected mercury halides due to spontaneous reduction or due to the reaction with ozone. Reduction of mercury because of reaction with the atmospheric ozone appeared to be the major cause of the sample loss and it was inherent in all tested materials at a comparable extent. We hypothesized the zirconia layer covered on a ceramic substrate (patented) to be less sensitive to the ozone-caused reduction, inert to gaseous elemental mercury and completely insensitive to atmospheric humidity. In addition, zirconia samplers were highly resistant to heating and they could be used for multiple adsorption/desorption cycles avoiding degradation in the atmospheric air. Key results of the zirconia sampler tests with mercury halides were: the collection efficiency of >98%; reduction with 50 ppb ozone in the first 4 min of exposition to the atmospheric air ─ 6% ±1%; spontaneous reduction at 50 °C in the first 4 min after spiking ─ <0.6%. Along with the above experimental results, some insights into the possible mechanism of interaction of ozone with mercury halides have been provided.

Being the most reactive of all chemical elements and the lightest member of halogen group, fluorine is found in the environment as fluoride. Both natural and anthropogenic activities are responsible for fluoride contamination in groundwater. Fluoride has dual effect on human health. While lower concentration (<0.5 mg/L) is responsible for dental fluorosis, higher concentration (>1.5 mg/L) leads to skeletal fluorosis and even death. The present review paper is aimed at providing detailed occurrence of fluoride pollution around the globe and in India. Among the different defluoridation techniques to remove excess fluoride from contaminated drinking water at both community and domestic levels, adsorption is found to be very effective due to its technical feasibility, simple characteristics and comparative low-cost nature. Various adsorbents have been tested for their ability to treat fluoride contaminated water, viz., activated carbon, activated alumina, soil, clay and a variety of waste materials. Since fluoride pollution of drinking water is a major concern of poor people as they cannot afford to spend on purification of water, usage of low-cost natural mineral (natural mineral) as adsorbent for fluoride removal is one of the most essential issues in modern era. The present review bestows a detailed discussion on natural mineral as adsorbent used in defluoridation process with special emphasis on soil and low-cost clay minerals.

In this study, activated red mud was used to develop an effective adsorbent in order to remove a toxic azo dye (tartrazine E102) from aqueous solutions. To increase the adsorption capacity, the red mud was activated by acid-heat treatment using 20 wt.% HCl (RM-HCl). To establish the optimum operating parameters, the influence of pH, adsorbent dose, contact time, initial dye concentration, and stirring rate was investigated. The adsorption equilibrium was studied using Langmuir, Freundlich, Dubinin-Radushkevich, Temkin isotherm models, and the characteristic parameters for each adsorption isotherm were determined. The kinetics of the adsorption process was analyzed by means of pseudo-first-order and pseudo-second-order models. The maximum removal efficiency obtained under optimum conditions was 84.72%. These results were in accordance with the isotherm and kinetic data. The results suggested that tartrazine adsorption process follows the pseudo-second-order kinetic model and also that fits Langmuir isotherm model. The maximum monolayer adsorption capacity was 136.98 mg/g.

The aim of this study was to investigate phosphate removal using crushed concrete granules (CCGs). The CCGs were thermally treated at different temperatures (300, 500, 700, and 900 °C) for 3 h under anoxic conditions. The results showed that CCGs thermally treated at 700 °C (700TT-CCGs) were the most effective for the removal of phosphate. The equilibrium adsorption data fitted well the Langmuir isotherm model with a maximum phosphate adsorption capacity of 21.522 mg/g, higher than that of granular adsorbents in the literature. In pH experiments, phosphate adsorption by 700TT-CCGs decreased as initial pH increased from 3 to 5, but sharply increased above pH 5 (final pH 9.1), which was favorable for the formation of calcium phosphate precipitate. The effect of competing anions on phosphate adsorption follows the order: HCO₃⁻ > SO₄²⁻ > NO₃⁻, which is consistent with the reverse order of the shared charge. Column experiments showed no breakthrough of phosphate in the column packed with half 700TT-CCGs and half sand for over 300 h. This study demonstrates that CCGs can be used for phosphate removal from aqueous solution after thermal treatment, which is a simple and cheap way to improve the phosphate removal capacity of CCGs.

Chicken feather, which is consisted of keratin, has always been abandoned as solid waste. The utilization technologies of waste keratin have been developed in electric zones and materials fields so far. Recently, numerous new types of adsorbents have been used for antibiotic removal. The chicken feather carbon is supposed to be a potential one. In this study, an activated feather carbon (AFC) was developed as the absorbent of amoxicillin (AMOX) in simulated wastewater. The micropore structures of AFC were detected by the scanning electron microscope (SEM). X-ray photoelectron spectrum (XPS) was recorded and analyzed. A BET surface area, as high as 1838.86 m²/g, was measured in this study. At the meantime, a rapid adsorption (5∼7 min) and high removal efficiency (99.63%) could be observed. The kinetics, isotherms, and thermodynamic studies indicated that the adsorption of AMOX by AFC was an exothermic physic-adsorption. The interaction between AMOX and AFC surface was supposed to be a multiple-layer adsorption process for it is well fitted with the Freundlich model. The adsorption behavior could be described by pseudo-second-order model almost perfectly in kinetic studies. In addition, effect of pH, ionic strength, and reusability properties were also discussed in this paper. The AFC was proved to be the most rapid, efficient, and economically absorbent for AMOX removal, which was effective enough under various temperatures and saline circumstances. It was also proved useful, convenient, and renewable in dealing with the tough antibiotic pollutant problems and rebuilding of antibiotic sewage treatment facilities.