Two-dimensional HPLC (2D-HPLC) recently has received great attention due to providing high resolving power and higher peak capacities than that of 1D-HPLC, especially dealing with a wide spectrum of sample matrices containing several components. In this work, an on-line heart-cutting two-dimensional liquid chromatography (2D-LC) method was developed using monolithic columns coupled with reversed-phase liquid chromatography (RPLC). 2D-HPLC was successfully carried out using affinity-based monolithic columns at first dimension (20 cm × 4.6 mm I.D.) followed by a Pinnacle II PAH column (50 mm × 4.6 mm I.D.) at the second dimension. Furthermore, good linearity was observed for the correlation of the benzo[a]pyrene (BaP) molecule against the peak areas (R² = 0.994) in the concentration range of 0.01–1.0 ng/mL in 30 min. The limit of detection and the limit of quantification were found to be 4.0 pg/mL and 12.0 pg/mL, respectively. Both the intra-day and inter-day precision at 0.01 and 0.1 ng/mL spiked concentrations were below than 2.35% RSD whereas the means of the recovery data of the BaP from the water samples were found to be in the range of 93.71–98.65%. These results demonstrate that the 2D-HPLC system, developed by the combination of the P(HEMA-MAPA) column and Pinnacle II PAH column, is reliable, stable, and well qualified in the extraction of polycyclic aromatic hydrocarbons from the water samples.

To elucidate the inhibitory effects of different herbicides on soil nitrification, eight widely used herbicides, i.e., acetochlor, atrazine, dicamba, isoproturon, paraquat, puma, tribenuron-methyl, and 2,4-dichlorophenoxyacetic acid butyl ester (2,4-Dbe), which represent different chemical taxonomy were selected. Our results indicated that herbicide 2,4-Dbe displayed the best inhibitory effect on nitrification, followed by puma and tribenuron-methyl, whereas the remaining five herbicides exhibited less effect when 10 mg of active ingredient (A.I.) of every herbicide per kg of soil was applied in vegetable-planting soil. The inhibition appeared when 5–100 mg of A.I. 2,4-Dbe was employed, which was enhanced with an increment in its dose in both vegetable-planting and fluvo-aquic soils. However, the inhibitory effect of 10 mg of A. I. 2,4-Dbe exhibited obvious differences in these two types of soils, where the duration of inhibition was shorter as it only continued about a week in fluvo-aquic and calcic cambisols soils with strong nitrification activity but poorer effect as compared to 10 mg of dicyandiamide (DCD). In contrast, the duration of inhibition exceeded 2 months in dryland red and shajiang black soils with a weak nitrification activity which was equivalent to DCD. In addition, comparing with five nitrification inhibitors, 10 mg of 2,4-Dbe had better inhibition than the substituted pyrimidine (AM) and sulfocarbamide (SU), but was equivalent to DCD, nitrapirin, and 3,4-dimethylpyrazole phosphate (DMPP) at their recommended application rates in dryland red soil. These obtained data clearly indicated that 2,4-Dbe could play a stronger role as a nitrification inhibitor in soils.

Worldwide, reef building corals are being degraded due to increasing anthropogenic pressure, and as a result, macroalgal cover is being increased. Hence, mechanism of coral–algal interaction, differential coral response to algal overgrowth, is critical from every geographical location to predict future coral dynamics. This paper documents the frequency of coral–algal (Halimeda) interactions, differential coral response to algal interaction. We found difference in susceptibility among coral genera to competitive effects. Out of 970 coral colonies surveyed, 36.7% were in contact with Halimeda sp. Most frequent contact was observed in Porites (57%) followed by Favites 28% (n = 60), Acropora 26% (n = 48), Platygyra 5% (n = 5) and Symphyllia 4.2% (n = 3). Frequent discoloration and tissue loss were only observed in Porites. Continuous monitoring revealed that long-term algal physical contact prevents light required for polyp for photosynthesis and stops coral feeding ability. In this study, we also found mutual exclusion between Halimeda and coral recruit. Out of 180 coral colonies (size class between 5 and 15 cm) comprised of Favites (n = 74), Acropora (n = 20), Favia (n = 79) and Porites (n = 7) surveyed, none of them were found in Halimeda-dominated sites. The documented effects of recruitment exclusion and tissue mortality followed by algal interaction on major reef building corals (Porites) could affect replenishing process and health of the remaining healthy corals in the Palk Bay reef if algal proliferation rate is not controlled through proper management strategies.

New optical tools are proposed for the real-time diagnosis of water quality without traditional sampling and laboratory physico-chemical analysis. In particular, the optical decision-making system is developed as an operational tool for in-situ assessment of water quality in natural water areas. Specifically, three versions of this system are analyzed using 8-channel and 35-channel photometric devices and a 128-channel spectroelipsometric device. The spectral images obtained from these devices are the basis for the diagnosis of water quality by using new algorithms to detect these spectral images. In more detail, four algorithms are developed to identify optical spectral images of water objects. The effectiveness of these optical tools is demonstrated in experimental water quality control sites in water systems operating under different climatic conditions. Finally, the results for the determination of the various pollutants at the surface of these water bodies are presented.

A challenge in side-stream treatment of anaerobic digester supernatant is that the effluent does not meet discharge standards. To address this challenge, this study tested tubular multichannel ceramic microfiltration (MF) and ultrafiltration (UF) membranes for the post-treatment of anaerobic digester supernatant. Pollutant rejection (total suspended solids (TSS), COD, total nitrogen (TN), and total phosphorus (TP)), color removal, and membrane susceptibility to fouling were determined at various transmembrane pressures (TMPs) (0.2, 0.3, 0.4, 0.5 MPa). Both methods completely removed TSS. In MF, COD was removed with 48–76% efficiency at 0.2–0.4 MPa. In UF, COD removal efficiency was slightly higher, reaching 83.7% at 0.4 MPa. With both methods, pollutant removal did not increase at TMP of 0.5 MPa. With both MF and UF, color was reduced by 54–100%, irrespective of the TMP. At 0.2–0.4 MPa, membrane resistance was lower and permeate flux was much higher with MF than UF. At 0.5 MPa, the methods differed only slightly from each other. Due to the larger cut-off, flux decline was slower in MF (0.7 h⁻¹) than in UF (1.1 h⁻¹), as the larger pore-size favors less foulant deposition. Thus, taking into account rejection efficiency, capacity, washing frequency, and cost (pressure), these results indicate that MF at 0.4 MPa is the most effective variant for post-treatment of anaerobic digester supernatant. With this variant, the almost colorless permeate contained 25 mg COD/L, no TSS, 55 mg TN/L (75% in the form of nitrites and nitrates), and 8.5 mg TP/L, thus meeting criteria for water to be used in irrigation or algae cultivation.

Polycyclic aromatic hydrocarbons (PAHs) upset the basic biological parameters of the soil, such as enzymatic activity, which can be used to identify the direction and intensity of organic and mineral substance transformation in the soil environment. The aim of this study was to determine the impact of soil contamination with naphthalene, phenanthrene, anthracene and pyrene at rates of 0–4000 mg kg⁻¹ DM (dry matter) of soil on the activity of acid phosphatase and alkaline phosphatase. An analysis was also conducted on how some organic substances, such as cellulose, sucrose and compost at rates of 0 and 9 g kg⁻¹ DM alleviate the PAH impact on the enzymes under study. The experiment was carried out in a laboratory with loamy sand as the soil material. Phosphatase resistance (RS) and soil resilience (RL) were calculated. The enzyme activity was found to depend significantly on the PAH rate, time of PAH deposition in soil and the type of organic substance added to the soil. The activity of acid and alkaline phosphatase increased with the degree of soil contamination with PAHs. Naphthalene had the greatest stimulating effect on enzyme activity. Biostimulation of soil with cellulose, sucrose and compost had a positive effect on acid and alkaline phosphatase activity, with cellulose and compost being the most effective in boosting acid and alkaline phosphatase activity, respectively. Naphthalene had the greatest effect on acid and alkaline phosphatase resistance and pyrene had the least effect. Low RL indices indicate that the presence of PAHs permanently disturbed the activity of acid and alkaline phosphatase.

This research work is focused on the synthesis, characterization, and application of cost-effective biochar–biopolymeric hybrid adsorbents from waste agricultural biomass and sodium alginate. The adsorbents were characterized by BET (Brunauer–Emmett–Teller), FTIR (Fourier transform infrared), XRD (X-ray diffraction), FESEM (field emission scanning electron microscopy), and bulk density measurement. The performance of the synthesized hybrid adsorbents has been tested for the removal of aqueous phase Ni²⁺ and Cu²⁺ metal ions at a concentration range of 25 to 100 mg/L, adsorbent dose of 1–3 g/L, and system temperature of 298–308 K, respectively. The effect of various physicochemical process parameters such as solution pH, adsorbent dose, initial metal ion concentration, temperature, and presence of salts on metal ion adsorption has been studied here, and experimental process parameters are being optimized by response surface methodology (RSM). The model was fitted well with the experimental data. Various kinetic models, namely, pseudo-first-order, pseudo-second-order, and Weber–Morris, have been fitted with batch experimental data, and the mechanism of adsorption has been identified. The maximum Langmuir monolayer adsorption capacity for Cu²⁺ and Ni²⁺ were 112 and 156 mg/g, respectively, which are comparative to other published adsorbent’s capacity data under similar experimental conditions. Thermodynamic parameter studies showed that the system was endothermic and spontaneous in nature.

Vertical variations of radionuclides, trace metals, and major elements were determined in two sediment cores, which were collected in the marine environment of Ierissos Gulf near Stratoni’s mining area. The enrichment factors (EFs) were also estimated and provided moderately severe to extremely severe enrichment for most trace elements and Mn, describing the anthropogenic influence in the gulf during the previous century. According to the applied dating models based on ²¹⁰Pb and ¹³⁷Cs, the effect in the marine sediment due to the exploitation of pyrite for the production of sulfuric acid during 1912–1920 was observed. Additionally, the decrease of mining activity during 1935–1945 due to the Second World War and the type of ore exploitation, the alteration of the exploited ores, and the construction and operation of Olympiada’s floatation plant during 1950–1970 were identified. The end of tailing discharging into the marine environment during 1980–2010 was also noted.

This paper reports the effects of single and combined application of biochar and phosphate fertilizer on immobilization of heavy metals in e-waste-contaminated soils. The results showed that combined amending biochar and phosphate fertilizer improved physical and chemical characteristics of soil but resulted in ammonium nitrogen loss. Biochar combined with phosphate fertilizer increased shoot biomass of lettuce while biochar applied alone could inhibit the growth of lettuce. A distinct decrease of heavy metal concentrations in lettuce was observed in phosphate fertilizer + biochar (3.0%) treatments while highest heavy metal concentrations in shoots and roots were observed in control treatments. In phosphate fertilizer (0.8%) + biochar (3.0%) treatment, Cd, Cu, Pb, and Zn concentrations of lettuce leaf were reduced by 34.78%, 29.37%, 46.59%, and 40.95%, respectively. Biochar + phosphate fertilizer and biochar both reduced bioconcentration of Cd, Cu, Pb, and Zn in different tissues of lettuce while transshipment of Cd, Cu, Pb, and Zn from root to shoot increased after combined amendment of biochar with phosphate fertilizer. Application of phosphate fertilizer + biochar enhanced the immobilization of Cd, Cu, Pb, and Zn by decreasing the exchangeable Cd, Cu, Pb, and Zn in the soil. Precipitation, adsorption, ionic exchange, and chelation contributed to the good immobilization capacity of biochar + phosphate fertilizer on Cd, Cu, Pb, and Zn in e-waste-contaminated soils.

Two materials (ZnO nanoparticles (nanZnO) and a composite (Ze-nanZnO)) were prepared; the composite was prepared by chemical precipitation on a natural zeolite. The materials were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), UV-Vis spectroscopy (UV-Vis), and Branauer-Emmett-Teller (BET) surface area. These materials were evaluated for the removal of tartrazine; this dye was used because it is considered a dangerous contaminant. All experiments were done in batch process. The effect of different parameters such as the contact time, the initial dye concentration, and pH, in addition to the thermodynamic parameters, were studied in order to determine the best experimental conditions. The nanZnO shows a higher adsorption capacity than the Ze-nanZnO composite; however, the separation of the phases was difficult when nanoparticles were used. According to the kinetic data, the mechanism for the nanZnO is physisorption and for the Ze-nanZnO composite is chemisorption. The results show that this is a useful technique for the removal of this dye.