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.

New approaches are required for prevention and control of biofilm-producing bacteria and consequently mitigating the health problems of bovine clinical mastitis. This work designed to determine prevalence rates of biofilm-producing bacteria that causing bovine clinical mastitis and evaluate the anti-biofilm effectiveness of novel nanocomposite of zinc–aluminum layered double hydroxide intercalated with gallic acid (GA) as chelating agent (Zn-Al LDH/GA) on the prevention and control of environmental pathogenic bacteria; Escherichia coli (E. coli), Klebsiella pneumoniae (K. pneumoniae), Staphylococcus aureus (S. aureus), and Coagulase-negative staphylococci (CNS), besides Listeria monocytogenes (L. monocytogenes) and assess the ability to use as an antimicrobial agent, and/or sanitizer for milking equipment. All samples (n = 230) involved clinical mastitis cow’s milk (n = 50) beside environmental samples (n = 180) were collected then examined for isolation and identification of bacterial pathogens. Zn-Al LDH/GA nanocomposite was synthesized using co-precipitation method, then characterized by Fourier-transform infrared spectroscopy (FT-IR); X-ray diffraction (XRD); field emission scanning electron microscopy (FESEM); high-resolution transmission electron microscopy (HRTEM); thermogravimetric analysis (TGA); differential thermal analysis (DTA); zeta potential; DLS analysis; and Brunauer, Emmett, and Teller (BET) surface area. The anti-biofilm activity of nanocomposite against mastitis-causing bacteria was detected using the broth micro-dilution and disc-diffusion assay. Results, the minimum concentration of Zn-Al LDH/GA that inhibited the growth of gram-positive and negative bacteria, were 312–625 and 5000 μg/mL, respectively. The LD₅₀ of Zn-Al LDH/GA was determined in mice at 1983.3 mg/kg b.wt. As a conclusion, Zn-Al LDH/GA nanocomposite proved its efficiency as an antimicrobial agent and/or sanitizer used for cleaning of milking equipment, due to it could inhibit the growth and multiplication of potentially pathogenic bacteria that causing clinical mastitis and its formation of biofilm on the milking equipment. Zn-Al LDH/GA was found to use under varying pH conditions compared with other commercial sanitizer used besides the formation of nanocomposite increases the material stability.

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.

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.

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.

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.

In this study, Mn-doped MgAl-layered double hydroxides (LDHs) were successfully synthesized for efficient removal arsenate from aqueous solution. The structure and composition of Mn-doped MgAl-LDHs intercalated by different ions such as CO₃²⁻, Cl⁻, or NO₃⁻ were investigated. The characterizations of XRD, ATR FT-IR, SEM, TG-DTA, and N₂ adsorption-desorption presented that the Mn-doped MgAl-LDHs (donated as Mn-LDHs) have very similar physical morphologies and properties to the MgAl-Cl-LDHs (donated as Mg-LDHs). However, the Mn-LDHs exhibits more preferable arsenate adsorption than Mg-LDHs. The As(V) removal kinetics data of Mn-LDHs is followed pseudo-second-order expression. The adsorption capacity of As(V) on Mn-LDHs via Langmuir isotherm model was 166.94 mg g⁻¹. The results of XPS revealed that the enhanced removal mechanism can be attributed to surface complexation of As(V) with Mn on the surface of Mn-LDHs. These results prove that Mn-doped LDHs can be considered as a potential material for adsorption As(V) from wastewater.

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