Phosphorus (P) recovery from sewage sludge (SS) have been regarded as an effective method of P recycling. The effects of incineration temperature, incineration time, and chlorine additives on the distribution of P speciation during sludge incineration were studied. Moreover, the reactions between model compounds AlPO₄ and additives (MgCl₂ and CaCl₂) were investigated by thermogravimetric differential thermal analysis and X-ray diffraction measurements. The results demonstrated that the increase in temperature and time stimulated the volatilization of non-apatite inorganic phosphorus (NAIP) instead of apatite phosphorus (AP). MgCl₂ and CaCl₂ can greatly promote the conversion of NAIP to AP. Additionally, AlPO₄ reacted with MgCl₂ are incinerated at 500–600 °C to form Mg₃(PO₄)₂, which is mainly due to the reaction of the intermediate product MgO and AlPO₄. Reactions between AlPO₄ and CaCl₂ occurred at 700–750 °C and produced Ca₂PO₄Cl, which can be directly used with high bioavailability. These findings suggested that chlorine additives in the SS incineration process can obtain phosphorus-containing minerals with higher bioavailability to realize the resource utilization of P in sludge.

Photosynthetic microalgal growth is a promising tool for mitigation of gaseous effluent from the cement production, which is highly implicated in global warming and climate change. We investigated the effects of actual cement industry flue gas on the physiology of Chlorella vulgaris under laboratory-controlled conditions. We evaluated the growth, photosynthetic performance, intracellular metal content, total proteins, and carbohydrates of C. vulgaris under three gas input rates: 9, 36, and 54 L d⁻¹; compressed air (54 L d⁻¹) was used as control. The results showed no correlation between the flue gas input rates on total proteins and carbohydrates in the algal biomass, and no effects on growth rates. However, rapid light curves indicated that the light use efficiency (α) and the maximum relative electron transport rate (rETRₘₐₓ) were stimulated when applying 9 and 36 L d⁻¹. Metal analysis revealed an accumulation of Cr, Zn, and Ni in the algal biomass exposed to flue gas (54 L d⁻¹) compared to the control. Thermogravimetry and differential thermal analysis showed that 70% of the cement kiln dust were composed by uncalcined limestone, which may have stimulated photosynthesis, as indicated by the rapid light curve parameters. In general, C. vulgaris can be considered a robust organism for cement flue gas bioremediation.

This study investigated methane (CH₄) adsorption by natural sepiolite—obtained from Eskisehir in Turkey—and its Ag-, Cu-, Fe-, and H-exchanged forms by using a volumetric gas adsorption method. Sepiolite was modified with 1 M AgNO₃, 1 M Cu(NO₃)₂∙3H₂O, 1 M Fe(NO₃)₃∙9H₂O, and 1 M HCl solutions at 80 °C for 6 h, respectively. The natural and modified sepiolite samples were characterized by using X-ray diffraction (XRD), X-ray fluorescence spectroscopy (XRF), Fourier transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TG-DTG), differential thermal analysis (DTA), and the nitrogen adsorption method. Quantitative XRD analysis showed that the sample consisted primarily of sepiolite clay mineral and dolomite as an impurity in small amounts. It was found that acid and heavy metal treatments caused apparent changes in the structure and microporosity of the sepiolite samples. CH₄ adsorption isotherms of clay samples were examined at temperatures of 0 °C and 25 °C and pressures up to 100 kPa. It was determined that the CH₄ adsorption capacities of sepiolite samples increased at both temperatures according to the following sequence: CuS < AgS < HS < S < FeS. CH₄ adsorption values of sepiolite samples varied between 0.084 mmol/g and 0.299 mmol/g. It was observed that the CH₄ adsorption capacities of heavy metal cation-exchange clay samples were related to the surface area.

ZnAl-layered double hydroxide-loaded banana straw biochar (ZnAl-LDH-BSB) was prepared via the hydrothermal method, and the efficient phosphorus removal agent ZnAl-LDO-BSB was obtained by calcination at 500 °C. Based on the ZnAl-LDO-BSB adsorption characteristics, the adsorption mechanism was evaluated via TG/DTA, FTIR, XRD, SEM, HRTEM, and other characterization methods. The results showed that the ZnAl-LDO-BSB assembled into microspheres with typical hexagonal lamellar structures and presented good thermal stability. The adsorption of total phosphate (TP) by ZnAl-LDO-BSB conforms to the Langmuir model, and the theoretical maximum adsorption capacity is 185.19 mg g⁻¹. The adsorption kinetics were in accordance with the second-order kinetic model, and the anion influence on TP adsorption followed the order CO₃²⁻ > SO₄²⁻ > NO₃⁻. The combination of zeta potential measurements with the FTIR, XRD, SEM, HRTEM, and XPS results suggested that ZnAl-LDO-BSB adsorbs TP mainly by electrostatic adsorption, surface coordination, and anion intercalation. Graphical abstract

In this study, we investigated the effects of SiO₂ nanoparticles (SiO₂-NPs) (1, 10, 25, 50, and 100 mg/L) for 24 h in vitro on the motility parameters and oxidative stress markers such as total glutathione (TGSH), catalase (CAT), and malondialdehyde (MDA) of rainbow trout, Oncorhynchus mykiss sperm cells. Therefore, SiO₂-NPs were synthesized with sol-gel reaction from tetraethoxy orthosilicate (TEOS). The prepared nanoparticle structures were characterized for chemical structure, morphology and thermal behavior employing Fourier transform infrared spectroscopy, X-ray spectroscopy, scanning electron micrograph, and thermal analysis (DTA/TGA/DSC) techniques. After exposure, there was statistically significant (p < 0.05) decreases in velocities of sperm cells. CAT activity significantly (p < 0.05) decreased by 9.6% in sperm cell treated with 100 mg/L. In addition, MDA level significantly increased by 70.4% and 77.5% in sperm cell treated with 50 and 100 mg/L SiO₂-NPs, respectively (p < 0.05). These results showed that SiO₂-NPs may have toxic effect on rainbow trout sperm cells in 50 mg/L and more.

The efficiency of the as-prepared Mg₀.₂₅Co₀.₇₅Fe₂O₄ spinel nanoparticles for adsorption of crude oil from aqueous solution was improved by blending them with chitosan hydrogel (CH) prepared using epichlorohydrin as cross-linker resulting (CH/Mg₀.₂₅Co₀.₇₅Fe₂O₄) nanocomposites. Mg₀.₂₅Co₀.₇₅Fe₂O₄ nanocrystals was prepared by the chemical co-precipitation method and characterized by using X-ray diffraction (XRD), infrared spectroscopy (FT-IR), scanning electron microscope (SEM), transmission electron microscope (TEM), and differential thermal analysis (DTA)/thermogravimetric analysis (TGA). DTA/TGA results showed that the net weight loss of the samples heated from room temperature up to 1000 °C lies in the range 2.2–26.5% weight, where the maximum weight loss appeared at 100 °C and 614 °C. The blending nanocomposites prepared, were characterized by FT-IR and SEM micrographs. The effect of the nanoparticles ratio on the water uptake of nanocomposites and their capability to adsorb the crude oil was estimated by the gravimetric method. TEM results showed that the average nanoparticle size (Z) of Mg₀.₂₅Co₀.₇₅Fe₂O₄ is 30.06 nm and the SEM illustrated the presence of a very clear and rough layer of pores which are homogenously arranged structures that could play an important role in the adsorption and stability of crude oil on polymers. The adsorption ability of crude oil from waste water on the CH/Mg₀.₂₅Co₀.₇₅Fe₂O₄ nanocomposites hydrogel was reported and it was found that the CH/Mg₀.₂₅Co₀.₇₅Fe₂O₄ with 95/5% ratio showed the improvement in the oil adsorption (72.5%) than the 0/100% one (50.2%). As a consequence, it is highly suggested that the potential of blending CH with Mg₀.₂₅Co₀.₇₅Fe₂O₄ to obtain CH/Mg₀.₂₅Co₀.75Fe2O₄ for enhancing crude oil adsorption in oily waste water treatment with a low cost.

Preparation of Ce₂(MoO₄)₃ nanoparticles is reported via the microemulsion method by using two different surfactants, i.e., cationic surfactant, cetyltrimethylammonium bromide (CTAB), and nonionic surfactant, Triton X-100. The water pools produced in the microemulsion systems behave as nanoreactors for reaction of the cerium (3+) and molybdate ions to produce Ce₂(MoO₄)₃ nanoparticles. The structure and morphology of the products were characterized by using Fourier-transform infrared (FT-IR) spectroscopy, energy-dispersive X-ray analysis (EDX), UV-Vis spectroscopy, X-ray diffraction (XRD), thermogravimetric analysis (TGA-DTA), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The prepared Ce₂(MoO₄)₃ nanoparticles were successfully utilized as photocatalysts to remove crystal violet from aqueous solution in which the maximum percentage of dye degradation was about 89% after 5 h under the visible light irradiation. Also, kinetic study of the photocatalytic degradation revealed that pseudo-second order model is the best one for describing kinetic of the reaction.

The present paper describes the sono-assisted adsorption (sono-adsorption) of methylene blue (MB), methyl violet (MV), and Nile blue (NB) from aqueous solution by AC/CoFe₂O₄ magnetic composite. FT-IR, TGA-DTG, VSM, XRD, TEM, SEM, EDX, Map, and Raman analysis were used to characterize the magnetic composite. The magnetization saturation value of AC/CoFe₂O₄ magnetic composite was determined to be 53.06 emu/g. Dye sono-adsorption efficiency was increased by increasing adsorbent dose, pH value, and contact time, but not dye concentration. Pseudo-first-order, pseudo-second-order, and intra-particle diffusion models were used to study the kinetic behavior of the cationic dye sono-adsorption. The sono-adsorption kinetics was reasonably followed by pseudo-second-order model (R² > 0.998). The results showed that the Freundlich model (R² > 0.976) was more able to describe the sono-adsorption equilibrium behavior than Langmuir, D-R, and Scatchard models. The maximum sono-adsorption capacity of NB, MV, and MB was determined as 86.24, 83.90, and 87.48 mg/g, respectively. Based on the parameters derived from isotherm modeling (RL, n, and E), the sono-adsorption process of cationic dyes is desirable and physical. An increase in NaCl concentration reduced the sono-adsorption efficiency for all dyes. Also, the adsorption-desorption of AC/CoFe₂O₄ magnetic was studied up to 10 stages, and it was confirmed that the sono-adsorption efficiency is acceptable up to the eight stage. AC/CoFe₂O₄ magnetic composite is, therefore, an affordable and recyclable adsorbent to remove the molecule of NB, MV, and MB dyes from aqueous media.

High concentrations of antibiotic compounds within pharmaceutical wastewater have hazardous impacts toward environment and human health. Therefore, there is an immediate requirement of efficient treatment method for removal of antibiotics from aquatic environment. In the present study, the cryptomelane catalyst-type manganese oxide octahedral molecular sieve (K-OMS-2) was synthesized in the presence of benzyl alcohol as a reducing agent and cetyltrimethylammonium bromide as a structure-directing agent and then utilized to reduce the metronidazole. The central composite design method was the experimental design adopted. The FESEM analysis revealed that the K-OMS-2 surface contained many uniformly cylindrical aggregates less than about 40 nm in diameter and about 80–100 nm in length. Besides, a high specific surface area of 129 m²/g and average pore size of 45.47 nm were recorded. According to the TGA/DTA analysis, the prepared catalyst revealed high thermal stability. The maximum metronidazole degradation (95.36%) was evident at conditions of pH = 3, catalyst mass = 0.97 g/L, contact time = 200 min, and metronidazole concentration = 20 mg/L. Metronidazole did not form a complex with nitrate, fluoride, sulfate, or hardness. These ions exerted a negligible effect on metronidazole reduction using the K-OMS-2 catalyst, except for hardness, which reduced the removal efficiency of metronidazole by 17%. The FTIR and LC-MS revealed a complex mechanism involved in the metronidazole degradation by the K-OMS-2 involving the formation of an amino group, a hydroxyelated compound via N-denitration, and hydrogenation process on the K-OMS-2 catalyst surface.

This study presents an efficient and facile method for biosynthesis of silver nanoparticles (AgNPs) and gold nanoparticles (AuNPs) using aqueous extract of burdock root (BR), A. lappa, and their applications. The nanoparticles were characterized by ultraviolet-visible spectrophotometry, X-ray diffraction, transmission electron microscopy, energy dispersive X-ray, thermogravimetry, and differential thermal analysis. AgNPs capped the BR extract (BR-AgNPs) possessed roughly spherical geometry with an average diameter of 21.3 nm while uneven geometry of AuNPs capped the BR extract (BR-AuNPs) showed multi shapes in average size of 24.7 nm. The BR-AgNPs strongly inhibited five tested microorganism strains. In particular, the nanoparticles showed excellent catalytic activity for the conversion of pollutants within wastewater. Pseudo-first-order rate constants for the degradation of 4-nitrophenol, methyl orange, and rhodamine B were respectively found 6.77 × 10⁻³, 3.70 × 10⁻³, and 6.07 × 10⁻³ s⁻¹ for BR-AgNPs and 6.87 × 10⁻³, 6.07 × 10⁻³, and 7.07 × 10⁻³ s⁻¹ for BR-AuNPs. Graphical abstract ᅟ