The sorption of two phthalate esters (PAEs) and phenanthrene (PHE) by different natural organic matter fractions (NOMs) was examined. The surface area of the NOMs correlated positively with the starting decomposition temperature (SDT), implying increased number of micropores with the rise of condensation. Sorption of PHE on nonhydrolyzable carbons (NHCs) and other NOMs was respectively dependent on aromatic and aliphatic C contents. Likely physical blocking of the aliphatic moieties and input of black carbon materials led to elevated sorption capacity for PHE of aromatic domains in the NHCs. Sorption of PAEs by NOMs excluding NHCs was jointly regulated by hydrophobic partitioning and H-bonding interactions. The SDT of the NOMs correlated negatively with the Koc when SDT ≥304 °C, likely because the highly condensed domains may impair the availability of amorphous moieties for sorption. This study highlights the influence of domain accessibility of NOMs on sorption of hydrophobic organic contaminants.

Understanding the trophic transfer of nanoparticles (NPs) is important because NPs are small enough to easily penetrate into organisms. In this study, we evaluated the trophic transfer of gold NPs (AuNPs) within the aquatic food chain. We observed AuNPs transfer from 2 species of primary producers (Chlamydomonas reinhardtii or Euglena gracilis) to the primary consumer (Daphnia magna). Also, bioaccumulation of AuNPs in E. gracilis was higher than that in C. reinhardtii. The reasons for the difference in Au accumulation may be the physical structure of these organisms, and the surface area that is available for interaction with NPs. C. reinhardtii has a cell wall that may act as a barrier to the penetration of NPs. The size of E. gracilis is larger than that of C. reinhardtii. This study demonstrates the trophic transfer of AuNPs from a general producer to a consumer in an aquatic environment.

The main aim of the present study was to estimate size segregated doses from e-cigarette aerosols as a function of the airway generation number in lung lobes. After a 2-second puff, 7.7 × 1010 particles (DTot) with a surface area of 3.6 × 103 mm2 (STot), and 3.3 × 1010 particles with a surface area of 4.2 × 103 mm2 were deposited in the respiratory system for the electronic and conventional cigarettes, respectively. Alveolar and tracheobronchial deposited doses were compared to the ones received by non-smoking individuals in Western countries, showing a similar order of magnitude. Total regional doses (DR), in head and lobar tracheobronchial and alveolar regions, ranged from 2.7 × 109 to 1.3 × 1010 particles and 1.1 × 109 to 5.3 × 1010 particles, for the electronic and conventional cigarettes, respectively. DR in the right-upper lung lobe was about twice that found in left-upper lobe and 20% greater in right-lower lobe than the left-lower lobe.

The properties of carbon nanotubes (CNTs) functionalized with –OH and –COOH groups during simulated water treatment with H2O2 and/or UV were tested. There following properties of CNTs were investigated: specific surface area, elemental composition (CHN), dynamic light scattering, Raman spectroscopy, X-ray photoelectron spectroscopy and changes in the CNTs structure were observed using transmission electron microscopy. Treatment of CNTs with H2O2 and/or UV affected their properties. This effect, however, was different depending on the functionalization of CNTs and also on the factor used (UV and/or H2O2). H2O2 plays a key role as a factor modifying the surface of CNT-OHs, whereas the properties of CNT-COOHs were most affected by UV rays. A shortening of the nanotubes, exfoliation, the opening of their ends, and changes in the surface charge were observed as a result of the action of UV and/or H2O2. The changes in observed parameters may influence the stability of the aqueous suspensions of CNTs.

The implications of biochar aging regarding their material properties as well as their interactions with other contaminants are not vivid. We report the role of biochar aging on sorption behavior of di-alkyl phthalates (PAEs). Biochars used in this study were produced from peanut-shell and their aging was simulated by chemical oxidation. The structural composition and morphology of the obtained biochars, before and after oxidation with HNO3/H2SO4, were analyzed by element composition, XPS, DRIFT, and SEM/EDX. Several experimental results unequivocally showed oxygen enrichment in the mixed acid treated samples compared to their precursors. Despite surface area reduction and pore destruction, increased PAEs sorption on oxidized biochar surfaces portrayed existence of strong PAEs binding sites. The adsorption of PAEs on oxidized biochar surface is a cumulative influence of hydrophobic interactions and pi–pi electron donor–acceptor interactions. Our results suggest that imminent aging of biochar upon environmental exposure may change their sorbent properties.

Small amounts (0.15wt%) of platinum and palladium were incorporated in porous, high surface area, ultra–stable H–USY–Zeolite by ion exchange method, and their catalytic activity was studied for carbon monoxide (CO) oxidation reaction, under various conditions of industrial importance. The catalyst was characterized by p–XRD, chemical analysis, SEM, TEM, evaluated for catalytic activity using a steady state, fixed bed catalytic reactor. The catalysts show high CO oxidation activity and it was possible to convert 0.044 mmols of CO per gram of catalyst at 120 °C, at a space velocity of 60 000 h−1 and with 100 ppm CO concentration in feed gas. The high catalytic activity of this noble metal catalyst also appears to be a factor of porous structure of zeolite facilitating mass transfer; high surface area as well as highly dispersed catalyst sites of palladium and platinum on zeolite structure. Introduction of acidic sites in zeolites probably makes them more resistant towards SO2, while their surface area and pore characteristics make this catalyst efficient even under high space velocity conditions, thus suggesting the potential of larger pore size zeolites over conventional porous materials for industrial applications.

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 scarcity of clean water affecting many parts of the world encourages efforts to improve water reclamation processes, which rely on their capability to remove diverse types of water pollutants and contaminants. Thus, this study reports the application of bamboo fiber powders as potential low-cost sorbent for removal of noxious organic compounds in aqueous solution. Bisphenol A, a biorefractory endocrine disruptor compound, was chosen as model compound in order to easily follow the separation process. Principal component analysis of the FTIR spectra and BET surface area measurements were performed on treated bamboo fiber powders. Treatment of the raw powders with alkali, ionic and non-ionic surfactants appeared to improve the bisphenol A removal performance of the bamboo fiber powders with the best removal efficiency reached at 39 % for a sorbent dosage of 4 g L⁻¹ gained after a bamboo treatment using the cationic surfactant. Effects of contact time, sorbent dosage, and particle sizes (55, 300, and 1000 μm) of cationic surfactant-treated bamboo fiber powders towards removal of bisphenol A were further assessed in a batch system with an optimum removal observed for 55 μm in particle size.

This paper analyzes the mathematical modeling procedure to describe the decomposition of adsorbed phenanthrene in prototypical and real soil samples (sand and agricultural soil, respectively) by ozone. The modeling scheme considered a set of ordinary differential equations with time varying coefficients. This model used the adsorbed ozone in the soil, the ozone reacting with the contaminant and the phenanthrene concentration in the soil sample. The main parameters involved in the mathematical model included a time varying ozone saturation function (k ₛₐₜ (t)) and reaction constants (k ᵣ). These parameters were calculated using the ozone concentration variation at the reactor output, named as ozonogram, and the measurements of phenanthrene decomposition through ozonation. The model was validated using two series of experiments: (1) soil saturated with ozone in the absence of the contaminant and (2) soil artificially contaminated with phenanthrene. In both cases, the proposed parametric identification method yields to validate the mathematical model. This fact was confirmed by the correspondence between numerical simulations and experimental data. In particular, total decomposition of phenanthrene adsorbed in two different systems (ozone-sand and ozone-agricultural soil) was obtained after 15 and 30 min of reaction, respectively. This difference was obtained as a consequence of soil physicochemical characteristics: specific surface area and pore volume. The ozonation reaction rate constants of phenanthrene in the sand and agricultural soil were calculated using the same parameter identification scheme.

Natural zeolitic tuff was modified with FeCl₃solution for the removal of fluoride, and the effect of chloride, nitrate, and sulfate ions was examined on fluoride sorption from solutions and drinking water. The unmodified zeolitic tuff (Z) and the iron-modified zeolitic tuff (Fe(III)-Z) were characterized by scanning electron microscopy and X-ray diffraction analysis. The elemental composition, the specific surface area, and the point of zero charge of the zeolitic material were also determined. The fluoride adsorption was carried out in a batch system considering the effect of contact time, the initial concentration of fluoride ions, and the effect of other anions naturally present in the drinking water. The kinetic and isotherm results were adjusted to the pseudo-second-order and Freundlich models, respectively, which indicated that the sorption mechanism was chemisorption on a heterogeneous material. The fluoride sorption capacity was higher in solutions (2.7 mg/g) than in drinking water (0.41 mg/g), and this could be attributed to the presence of other anions. Overall, the presence of chloride ions significantly diminished the fluoride adsorption capacity, while the presence of nitrate and sulfate ions did not show any significant effect; the anion removal efficiency by Fe(III)-Z followed the order F⁻ > > Cl⁻ > NO₃⁻ > SO₄²⁻.