Extracellular polymeric substances (EPS) found in soils can reduce the mobility of heavy metals through the use of both electrostatic and non-electrostatic mechanisms. Their effects vary from one soil type to another. The influence of EPS from Escherichia coli on the adsorption behaviors of Cu(II) and Cd(II) by two bulk variable charge soils, Oxisol and Ultisol, was studied at constant and varied pH, and the results were compared to a constant charge Alfisol. The maximum adsorption capacities of the soils were significantly (P < 0.05) enhanced in the presence of EPS, with Cu(II) adsorption being greater. Interaction of EPS with soils made the soil surface charge more negative by neutralizing positive charges and shifting the zeta potentials in a negative direction: from −18.6 to −26.4 mV for Alfisol, +5.1 to −22.2 mV for Oxisol, and +0.3 to −28.0 mV for Ultisol at pH 5.0. The adsorption data fitted both the Freundlich and Langmuir isotherms well. Preadsorbed Cd(II) was more easily desorbed by KNO₃ than preadsorbed Cu(II) from both the control and EPS treated soils. The adsorption of both metals was governed by electrostatic and non-electrostatic mechanisms, although more Cu(II) was adsorbed through the non-electrostatic mechanism. The information obtained in this study will improve our understanding of the mechanisms involved in reducing heavy metals mobility in variable charge soils and hence, their bioavailability.

Microplastics are an emerging contaminants of concern in aquatic environments. The aggregation behaviors of microplastics governing their fate and ecological risks in aquatic environments is in need of evaluation. In this study, the aggregation behavior of polystyrene microspheres (micro-PS) in aquatic environments was systematically investigated over a range of monovalent and divalent electrolytes with and without natural organic matter (i.e., Suwannee River humic acid (HA)), at pH 6.0, respectively. The zeta potentials and hydrodynamic diameters of micro-PS were measured and the subsequent aggregation kinetics and attachment efficiencies (α) were calculated. The aggregation kinetics of micro-PS exhibited reaction- and diffusion-limited regimes in the presence of monovalent or divalent electrolytes with distinct critical coagulation concentration (CCC) values, followed the Derjaguin-Landau-Verwey-Overbeek (DLVO) theory. The CCC values of micro-PS were14.9, 13.7, 14.8, 2.95 and 3.20 mM for NaCl, NaNO3, KNO3, CaCl2 and BaCl2, respectively. As expected, divalent electrolytes (i.e., CaCl2 and BaCl2) had stronger influence on the aggregation behaviors of micro-PS as compared to monovalent electrolytes (i.e., NaCl, NaNO3 and KNO3). HA enhanced micro-PS stability and shifted the CCC values to higher electrolyte concentrations for all types of electrolytes. The CCC values of micro-PS were lower than reported carbonaceous nanoparticles CCC values. The CCC[Ca2+]/CCC [Na+] ratios in the absence and presence of HA at pH 6.0 were proportional to Z−2.34 and Z−2.30, respectively. These ratios were in accordance with the theoretical Schulze–Hardy rule, which considers that the CCC is proportional to z−6–z−2. These results indicate that the stability of micro-PS in the natural aquatic environment and the possibility of significant aqueous transport of micro-PS.

Extracellular Polymeric Substances (EPS) influenced Poly Cyclic Aromatic Hydrocarbons (PAHs) degrading Klebsiella pneumoniae was isolated from the marine environment. To increase the EPS production by Klebsiella pneumoniae, several physicochemical parameters were tweaked such as different carbon sources (arabinose, glucose, glycerol, lactose, lactic acid, mannitol, sodium acetate, starch, and sucrose at 20 g/L), nitrogen sources (ammonium chloride, ammonium sulphate, glycine, potassium nitrate, protease peptone and urea at 2 g/L), different pH, carbon/nitrogen ratio, temperature, and salt concentration were examined. Maximum EPS growth and biodegradation of Anthracene (74.31%), Acenaphthene (67.28%), Fluorene (62.48%), Naphthalene (57.84%), and mixed PAHs (55.85%) were obtained using optimized conditions such as glucose (10 g/L) as carbon source, potassium nitrate (2 g/L) as the nitrogen source at pH 8, growth temperature of 37 °C, 3% NaCl concentration and 72 h incubation period. The Klebsiella pneumoniae biofilm architecture was studied by confocal laser scanning microscopy (CLSM) and scanning electron microscope (SEM). The present study demonstrates the EPS influenced PAHs degradation of Klebsiella pneumoniae.

The generation of HONO and NO₂ by the photolysis of nitrates in the presence of humic acids (HA) was measured under various conditions. The photolysis experiments of HA, KNO₃ and KNO₃/HA under simulated sunlight was carried out by a flow tube reactor at ambient temperature and pressure. HONO and NO₂ were major products by the photolysis of KNO₃. By contrast, the photolysis of HA and KNO₃/HA mainly generated HONO. HA significantly enhanced the formation of HONO during the photolysis process of KNO₃. With increasing the KNO₃ mass, the HONO formation rate (RHONO) on KNO₃/HA increased while the photolysis rate normalized by the KNO₃ mass exhibited an opposite trend. RHONO on KNO₃/HA linearly increased with irradiation intensity (88–262 W/m²) and relative humidity (7–70%), whereas it linearly decreased with the pH (pH = 2–12). In addition, the reaction paths of the HONO formation by the photolysis of nitrates in the presence of HA were proposed according to experimental results. Finally, atmospheric implications of the enhanced HONO formation by the photolysis of nitrates in the presence of HA were discussed.

Mediterranean coastal regions are particularly exposed to oil pollution due to extensive industrialization, urbanization and transport of crude and refined oil to and from refineries. Bioremediation of contaminated beach sand through landfarming is both simple and cost-effective to implement compared to other treatment technologies. The purpose of the present study was to investigate the effect of alternative nutrients on biodegradation of crude oil contaminated beach sand in an effort to reduce the time required for bioremediation employing only indigenous hydrocarbon degraders.A natural sandy soil was collected from Agios Onoufrios beach (Chania, Greece) and was contaminated with weathered crude oil. The indigenous microbial population in the contaminated sand was tested alone (control treatment) or in combination with inorganic nutrients (KNO3 and K2HPO4) to investigate their effects on oil biodegradation rates. In addition, the ability of biosurfactants (rhamnolipids), in the presence of organic nutrients (uric acid and lecithin), to further stimulate biodegradation was investigated in laboratory microcosms over a 45-day period.Biodegradation was tracked by GC/MS analysis of aliphatic and polycyclic aromatic hydrocarbons components and the measured concentrations were corrected for abiotic removal by hopane normalizations. It was found that the saturated fraction of the residual oil is degraded more extensively than the aromatic fraction and the bacterial growth after an incubation period of approximately 3weeks was much greater from the bacterial growth in the control.The results show that the treatments with inorganic or organic nutrients are equally effective over almost 30days where C12–C35n-alkanes were degraded more than 97% and polyaromatic hydrocarbons with two or three rings were degraded more than 95% within 45days. The results clearly show that the addition of nutrients to contaminated beach sand significantly enhanced the activity of indigenous microorganisms, as well as the removal of total recoverable petroleum hydrocarbons (TRPH) over a 45-day study period.

Possible environmental effects of flash powder mixture combustion containing aluminium and boron along with other ingredients like potassium nitrate and sulphur are reported. Once the firecrackers are lighted, they burst out particulate matter and harmful gases with scintillating effect. These particulate matters and the harmful gases together make the environment fogged and get deposited on all surfaces. Recent research suggests replacing aluminium with boron to implement safety during manufacturing and to enhance performance. But the effects of the combustion residue have to be checked and compared before implementation. Hence, in this work, the possible effects of the firework mixtures particularly flash powder mixtures containing aluminium are monitored and compared with the effects of boron blended flash powder mixtures. Based on the smoke settling test, plant growth test and soil test, it is concluded that up to 12.5% of boron can be added in flash powder mixture to prevent pollution of the environment. The threshold quantity of residue without affecting the soil quality for 100 % usage of boron was found as 10 g of residue in 2 kg of soil.

The use of reclaimed water (RW) for irrigation alleviates agricultural water shortages. However, N₂O emissions and N fertilizer transformations in soils irrigated with RW under different N fertilizer types and soil moisture contents are poorly understood. A 216-h laboratory incubation experiment was conducted to evaluate the effects of irrigation water types (RW and fresh water, FW), N fertilizer types (¹⁵N-labeled KNO₃ and (NH₄)₂SO₄), and soil moisture contents at 40, 60, and 90 % water-filled pore space (WFPS) on N₂O emissions and N fertilizer transformations in intact soil cores. The results showed that cumulative N₂O emissions ranged from 3.78 to 36.30 mg N m⁻², and fertilizer-derived N₂O losses accounted for 0.14–2.44 % of N fertilizers, while fertilizer-derived N residues (NO₃ ⁻-N + NH₄ ⁺-N) accounted for 10.16–26.95 % of N fertilizers. The N₂O emissions at 40 % WFPS and fertilizer-derived N residues at 60 % WFPS in soils irrigated with RW were significantly (10.98 and 20.95 %, respectively) higher than those irrigated with FW, while fertilizer-derived N₂O losses at 60 % WFPS in soils irrigated with RW were 10.26 % higher than those irrigated with FW. The N₂O emissions and fertilizer-derived N₂O losses in soils amended with (NH₄)₂SO₄ at 40 and 60 % WFPS were significantly (26.61–178.84 %) larger than those amended with KNO₃, while fertilizer-derived N residues in soils amended with KNO₃ were significantly (41.47 %) higher than those amended with (NH₄)₂SO₄. The N₂O emissions significantly increased with increasing soil moisture content. Our results indicate that N fertilizer types and soil moisture contents are the two important factors regulating N₂O emissions and N fertilizer transformations. When RW irrigation is used, controlling soil moisture contents within 41 and 60 % WFPS (the optimum is 46 % WFPS) and application of KNO₃ can reduce N₂O emissions and fertilizer-derived N₂O losses, and correspondingly increase fertilizer-derived N residues, which can contribute to climate change mitigation.

Accumulation of divalent manganese (Mn) and its toxicity in the green alga Scenedesmus quadricauda was studied at circumneutral pH (6.5). A comparison of two applied concentrations (10 or 100 μM) of MnCl₂, MnSO₄, and Mn(NO₃)₂ indicated that mainly sulfate evoked higher Mn accumulation. On the other hand, nitrate rather depleted antioxidative enzyme activities (APX, CAT, SOD), leading to an increase in ROS formation as proven by fluorescence microscopy. Subsequent experiments revealed that increase in pH (from 4.5 to 9.5) increased also Mn content but typically depleted amounts of reduced glutathione and phytochelatin 2. We also measured the size of particles formed from the manganese salts at pH 9.5. Competitive experiment between Ca/K salts (CaCl₂, CaSO₄, Ca(NO₃)₂, KCl, K₂SO₄, KNO₃) and Mn (as Mn sulfate) showed a negative relation between Ca and Mn amount but KNO₃ stimulated Mn accumulation. Microscopy revealed that mainly K salts elevated plasma membrane damage (Acridine orange staining). Data indicate that not only pH but also accompanying anion affects Mn accumulation and that Ca salts may affect Mn toxicity.

The effects of urea, (NH₄)₂SO₄, KNO₃, and NH₄NO₃ on nitrous oxide (N₂O) emission from soil at field capacity and submerged condition were studied during 120 days in the laboratory. Soils in both moisture regimes gave higher emissions in the beginning, which were reduced later. Total emission of N₂O was higher at submergence as compared to field capacity regardless of fertilizer type. At field capacity soil fertilized with ureaemitted the highest amount of N₂O (1903 μg N₂O-N kg⁻¹ soil) during 120 days while at submerged condition, soil with NH₄NO₃ gave the highest emission (4843 μg N₂O-N kg⁻¹ soil). In another study, the efficacy of seven nitrification inhibitors in reducing the emission of N₂O-N from soil fertilized with urea was tested in the laboratory. Nitrapyrin, 2-amino-4-chloro-6-methylpyrimidine (AM), and dicyandiamide (DCD) reduced the emission to 12, 24, and 63% that of urea, respectively, whereas sodium thiosulphate, sulphur, acetylene,and thiourea had no effect on emission of N₂O. In submerged conditions none of the inhibitors reduced the emission.

Coal fly ash (CFA) and coal-based incense sticks ash (ISA) have several similarities and differences due to the presence of coal as a common component in both of them. CFA are produced from the combustion of pulverized coal during electricity production in the thermal power plants while ISA are produced from the burning of incense sticks at religious places and at houses. A typical black colored Indian, incense sticks are mainly are comprised of coal powder or potassium nitrate, wood chip, fragrance, binder or binding agent, and bamboo sticks. The black colored incense sticks have coal powder or charcoal as a facilitator for smoother burning of incense sticks. The detailed investigation of CFA and ISA by X-ray fluorescence spectroscopy (XRF), electron diffraction spectroscopy (EDS), inductively coupled plasma-atomic emission spectroscopy (ICP-AES), Fourier transform-infrared (FTIR), X-ray diffraction (XRD), particle size analyzer (PSA), field emission scanning electron microscopy (FESEM), and transmission electron microscopy (TEM) revealed the morphological, chemical, and elemental properties. Both the coal based ashes comprises minerals like calcites, silicates, ferrous, alumina, and traces of Mg, Na, K, P, Ti, and numerous toxic heavy metals as confirmed by the XRF, ICP-AES, and EDS. While, microscopy revealed the presence of well-organized spherical shaped particles, namely cenospheres, plerospheres, and ferrospheres of size varying from 0.02 μm to 7 microns in CFA. Whereas, ISA particles are irregular, aggregated, calcium to carbon rich whose size varies from 60 nm to 9 microns and absence of well-organized spherical structures. The well developed and crystalline structure in CFA is due to the controlled combustion parameter in thermal power plants during the burning of coal while incense sticks (IS) burning is under uncontrolled manner. So, FTIR and XRD confirmed that the major portion of fly ash constitutes crystalline minerals whereas ISA have mainly amorphous phase minerals. CFA have ferrospheres of both rough and smooth surfaced, which was absent from the ISA and hence ferrous particles of CFA are of high magnetic strength. The detailed investigation of ashes will lead to the applications of ashes in new fields, which will minimize the solid waste pollution in the environment.