LSER models for organic compounds adsorption by single and multi-walled carbon nanotubes and activated carbon were successfully developed. The cavity formation and dispersion interactions (vV), hydrogen bond acidity interactions (bB) and π-/n-electron interactions (eE) are the most influential adsorption mechanisms. SWCNTs is more polarizable, less polar, more hydrophobic, and has weaker hydrogen bond accepting and donating abilities than MWCNTs and AC. Compared with SWCNTs and MWCNTs, AC has much less hydrophobic and less hydrophilic adsorption sites. The regression coefficients (e, s, a, b, v) vary in different ways with increasing chemical saturation. Nonspecific interactions (represented by eE and vV) have great positive contribution to organic compounds adsorption, and follow the order of SWCNTs > MWCNTs > AC, while hydrogen bond interactions (represented by aA and bB) demonstrate negative contribution. These models will be valuable for understanding adsorption mechanisms, comparing adsorbent characteristics, and selecting the proper adsorbents for certain organic compounds.

Natural soil montmorillonite and kaolinite nanoparticles (NPs) were tested as efficient sorbents for organic contaminant (OC) removal through mimicking their natural environmental dispersive states. Sorption of both mineral NPs decreased with increasing pH with ionizable pentachlorophenol (PCP), but increased with pH with non-ionizable phenanthrene (PHE), within the pH range of 4–10. In contrast, sorption decreased consistently for both PCP and PHE, as a function of increasing ion concentration (0.001–0.1 mol L−1). Sorption differences were likely caused by the electrolytic conditions dependent upon surface chemistry of OCs and mineral NPs. The results confirmed that the highly dispersive soil mineral NPs would prevail over both engineered NPs and their regular μm-sized colloids for OC removal, due to their ecological advantages and higher sorption properties. This finding provided a realistic assessment of the environmental function of soil natural minerals in water once they are released from soil into OC polluted aqueous systems.

Adsorption by carbonaceous sorbents is among the most feasible processes to remove perfluorooctane sulfonic (PFOS) and carboxylic acids (PFOA) from drinking and ground waters. However, carbon surface chemistry, which has long been recognized essential for dictating performance of such sorbents, has never been considered for PFOS and PFOA adsorption. Thus, the role of surface chemistry was systematically investigated using sorbents with a wide range in precursor material, pore structure, and surface chemistry. Sorbent surface chemistry overwhelmed physical properties in controlling the extent of uptake. The adsorption affinity was positively correlated carbon surface basicity, suggesting that high acid neutralizing or anion exchange capacity was critical for substantial uptake of PFOS and PFOA. Carbon polarity or hydrophobicity had insignificant impact on the extent of adsorption. Synthetic polymer-based Ambersorb and activated carbon fibers were more effective than activated carbon made of natural materials in removing PFOS and PFOA from aqueous solutions.

A high selective pre-treatment method for the extraction and analysis of mebendazole in environmental water samples was developed based on molecularly imprinted solid-phase extraction (MISPE). The mebendazole imprinted polymers were synthesized in acetonitrile using methacrylic acid and ethylene glycol dimethacrylate as functional monomer and cross-linker respectively. The imprinted materials showed high adsorption ability for mebendazole and were applied as special solid-phase extraction sorbents for selective separation of mebendazole. An off-line MISPE procedure was developed for the purification and enrichment of mebendazole from natural seawater samples prior to high-performance liquid chromatography analysis. The recoveries of spiked seawater on the MISPE cartridges were from 83.0% to 90.6%, and the values of the relative standard deviation were in the range of 2.78–4.13% (n=3). The satisfied results showed that this pre-treatment methodology for extracting mebendazole in seawater was simple and effective.

A mechanically robust and high-capacity oil sorbent is prepared by electrospinning a blend of polystyrene (PS) and polyacrylonitrile (PAN). The morphology, oil sorption capacity and mechanical property of the fibers formed in different compositions are investigated in detail. It is shown that the oil sorption capacity is a result of both the chemical composition and the specific surface area which related to diameter size. The addition of PAN as a component in fibrous sorbents can significantly improve the mechanical properties of PS fibers. Moreover, the oil sorption capacity increases with decreasing fiber diameter. The results also show that the maximum sorption capacities of the PS/PAN sorbent for pump oil, peanut oil, diesel, and gasoline were 194.85, 131.70, 66.75, and 43.38gg−1, respectively. Additionally, the sorbent exhibits quick oil sorption speed as well as high buoyancy, which make it a promising candidate for use as an oil spill cleanup sorbent.

The objective of this study was to investigate the chemisorption mechanisms of Cu(II) on alcohol functionalized carbon nanotubes (OH-CNT) compared to granulated activated carbon (F-400). Two different sizes of OH-CNT were used on both adsorption isotherm experiments and continuous-flow fixed-bed columns. The experiments were conducted as a function of adsorbent type with fixed bed height (5 cm), fixed flow rate (0.035 mL/min), and one initial Cu(II) concentration (10 mg/L) at pH 5.1 and room temperature. Isotherm curves follow Freundlich model with better adsorption capacity for OH-CNT (6.3 and 15.7 mg/g) compared to F-400 (6.0 mg/g). Breakthrough curves for all adsorbents were typical, while OH-CNT showed higher capacity to treat water per amount of adsorbent than F-400. After 5 days of desorption, there was very little Cu(II) leached from the OH-CNT column as compared to F-400 that slowly desorbed 85 % of Cu(II). These results indicated chemisorption process on OH-CNT with low residual release of Cu(II) from adsorbent after reaching saturation. A systematic correlation method using converted FTIR absorbance curves (first derivative analysis) of as-received and hybrid OH-CNT identified new peaks on the spectra for Cu(II) chemisorbed on CNT surface, showing that Cu(II) target acidic functional groups during adsorption.

Natural contamination has become a challenging problem in drinking water production due to metal contamination of groundwater throughout the world, and arsenic and chromium are well-known toxic elements. In this study, iron oxide-coated sand (IOCS) and granular ferric hydroxide (GFH) were used to study the effects of fulvic acid (FA) on the adsorptive removal of Cr(VI) and As(V) from synthetic groundwater. IOCS and GFH were characterized by SEM/EDS, and experiments were performed at different pH levels (6, 7, and 8). The surface of IOCS and GFH showed a high content of Fe and O (75 and 60 % of the atomic composition, respectively), suggesting that they can highly effectively adsorb Cr(VI) and As(V). Adsorption tests with the simultaneous presence of As(V) and FA, on the one hand, and Cr(VI) with FA, on the other hand, revealed that the role of FA on chromate and arsenate adsorption was insignificant at almost all pH values investigated with both adsorbents. A small influence as a result of FA was only observed for the removal of As(V) by IOCS at pH 6 with a decrease of 13 and 23 % when 2 and 5 mg/l were added to the synthetic water, respectively. It was also found that organic matter (OM) was leached from the IOCS during batch adsorption experiments. The use of FEEM revealed that humic-like, fulvic-like, and protein-like organic matter fractions are present on the IOCS surface.

The feasibility of date seeds as a new low-cost natural adsorbent for the removal of dissolved organic carbon (DOC) from oily produced water was investigated. The aim of this study was to elucidate the mechanism associated with the removal of DOC and to find the best equilibrium isotherms and kinetic models for DOC removal in batch adsorption experiments. The effect of various physicochemical parameters such as initial DOC concentration (18.5–93.5 mg/L), solution pH (4–9), temperature (25–45 °C), and date seeds dosages (0.5–2.0 g) was evaluated. The equilibrium stage was attained after a contact time of 120 min. The maximum DOC removal was 82 % for 93.5 mg/L of DOC concentration. The equilibrium data were well represented by the Langmuir isotherm. The maximum monolayer adsorption capacity of date seeds was found to be 74.62 mg/g. The separation factor, R L, from the Langmuir equation and the Freundlich constant, n, indicated a favorable adsorption. The kinetic studies indicated that the adsorption process follows the pseudo-second-order kinetics. The adsorption of DOC is governed by both surface and pore diffusion. The results revealed that the DOC uptake decreases when temperature and pH increases. The adsorption process has been found exothermic in nature, and the thermodynamic parameters were determined. The Langmuir isotherm model equation was adopted to design a single-stage batch absorber for DOC adsorption onto date seeds. The study demonstrated that date seeds can be considered as a promising low-cost adsorbent for the removal of DOC from oily produced water.

In this study, natural calcium-rich attapulgite (NCAP) was used to develop a low-cost adsorbent for removing fluoride (F⁻) from contaminated water. The results showed that calcination can dramatically increase the F⁻ sorption capacity of NCAP and that the maximum F⁻ sorption capacity occurred at 700 °C. The sorption of F⁻ on NCAP heated at 700 °C (NCAP700) followed pseudo-second-order kinetics and was described by the Langmuir equilibrium model. The estimated F⁻ sorption capacity was approximately 140.0 mg/g at pH 8.0, which was comparable with the sorption capacities of some nanomaterials. The sorption of F⁻ on NCAP700 performed well at pH values of 7 to 10. In addition, anions such as NO₃ ⁻ and SO₄ ²⁻ did not affect fluoride removal, but PO₄ ³⁻ and HCO₃ ⁻ moderately influenced fluoride removal. A column study conducted using NCAP700 with a particle size of 0.2–0.5 mm indicated that the adsorbent could effectively purify nearly 200 bed volumes (BV) of water containing 3.0 mg F/l at pH 8.5. The removal of F⁻ from water mainly resulted from the formation of calcium fluoride precipitates and the complexation of fluoride with the –OH group of NCAP700, which was further confirmed by scanning electron microscopy–energy dispersive spectrometry (SEM-EDS) and X-ray photoelectron spectroscopy (XPS).

Biosorption is a low-cost green technology for water pollution decontamination. Recently, new adsorbent materials (raw or modified) were synthesized and tested in a wide variety of different pollutants. Among them, researchers pay attention on an alternative use of composts. The major use of composts is as soil amendments to improve the fertility of soils. For the first time in literature, the present review article gathers information about the applicability of compost materials as biosorbents in batch modes. For this purpose, equilibrium modeling and isotherm, kinetic, and thermodynamic studies were discussed in details. Moreover, many parameters such as temperature, pH, and contact time were also analyzed. The main pollutants studied in this work are dyes and heavy metals either in single- or multi-component systems.