Enhancing soluble phosphorus removal within buffer strips using industrial by-products

Using industrial by-products (IBPs) in conjunction with buffer strips provides a potentially new strategy for enhancing soluble phosphorus (P) removal from agricultural runoff. Here, we investigate the feasibility of this approach by assessing the P sorption properties of IBPs at different solution-IBPs contact time (1–120 min) and solution pH (3, 5.5, 7.5), as well as possible adverse environmental effects including P desorption or heavy metal mobilisation from IBPs. Batch experiments were carried out on two widely available IBPs in the UK that demonstrated high P sorption capacity but different physicochemical characteristics, specifically ochre and Aluminium (Al) based water treatment residuals (Al-WTR). A series of kinetic sorption–desorption experiments alongside kinetic modelling were used to understand the rate and the mechanisms of P removal across a range of reaction times. The results of the kinetic experiments indicated that P was initially sorbed rapidly to both ochre and Al-WTR, followed by a second phase characterised by a slower sorption rate. The excellent fits of kinetic sorption data to a pseudo-second order model for both materials suggested surface chemisorption as the rate-controlling mechanism. Neither ochre nor Al-WTR released substantial quantities of either P or heavy metals into solution, suggesting that they could be applied to buffer strip soils at recommended rates (≤30 g kg^?1 soil) without adverse environmental impact. Although the rate of P sorption by freshly-generated Al-WTR applied to buffer strips reduced following air-drying, this would not limit its practical application to buffer strips in the field if adequate contact time with runoff was provided.     

Effect of nuclear power on CO<Subscript>2</Subscript> emission from power plant sector in Iran

Introduction  

It is predicted that demand for electricity in Islamic Republic of Iran will continue to increase dramatically in the future due to the rapid pace of economic development leading to construction of new power plants. At the present time, most of electricity is generated by burning fossil fuels which result in emission of great deal of pollutants and greenhouse gases (GHG) such as SO₂, NO_x, and CO₂. The power industry is the largest contributor to these emissions. Due to minimal emission of GHG by renewable and nuclear power plants, they are most suitable replacements for the fossil-fueled power plants. However, the nuclear power plants are more suitable than renewable power plants in providing baseload electricity. The Bushehr Nuclear Power Plant, the only nuclear power plant of Iran, is expected to start operation in 2010. This paper attempts to interpret the role of Bushehr nuclear power plant (BNPP) in CO₂ emission trend of power plant sector in Iran.     

Investigating the phenol removal from aqueous media by photocatalytic magnetized graphene oxide nanocomposite

As a large and diverse group of secondary metabolites, phenolic compounds are one of the most common chemical pollutants present in water resources. these compounds can have toxic effects on ecosystems and humans. Therefore, their removal from water sources appears to be of great importance. In this study, a magnetic graphene oxide (MGO) photocatalyst was synthesized and used to remove phenol from water. The fabricated GO magnetic nanocomposites were determined by SEM and FTIR techniques. Afterward, these nanoparticles were used to remove phenol from aquatic media considering different operational parameters, including pH of the solution, initial concentration of phenol, contact time, and adsorbent dosage. The results showed that the magnetized GO nanoparticles could remove 90.83% of phenol molecules under the optimal conditions of solution pH = 3.0, initial phenol concentration of 20 mg/L, adsorbent concentration of 300 mg/L, and contact time of 120 min. additionally have compared the results of UV, Fe₃O₄/GO, and Fe₃O₄/GO/UV on the removal of phenol under optimum conditions. Accordingly, the phenol removal efficiencies for UV alone, Fe₃O₄/GO, and Fe₃O₄/GO/UV were obtained at 4.5, 65.73, and 90.83%, respectively. Based on the findings, the prepared magnetic GO nanoparticles have extended capabilities such as easy and rapid separation from sample and high potential in removing phenolic compounds, so, it can be introduced as an appropriate adsorbent for removal of this pollutant from water and wastewater.     

Silica-supported antimony(III) chloride as a mild and reusable catalyst for the Paal–Knorr pyrrole synthesis

Heterogeneous catalysts are used for control of environmental pollution. Heterogeneous catalysts are easily separated from the reaction mixture, thus allowing their recovery and re-use. There is a need for catalysts that are efficient under mild conditions. Here, we show that silica-supported antimony(III) chloride (SbCl₃/SiO₂) acts as a highly efficient heterogeneous Lewis acid catalyst for the Paal–Knorr pyrrole synthesis at room temperature. We found that condensation of hexane-2,5-dione with aromatic and aliphatic primary amines in hexane using SbCl₃/SiO₂ with 7.6 wt% SbCl₃ was the best reaction condition. The silica support facilitated the workup of the reaction mixture and provided a reusable catalyst at least for 7 runs without significant loss in activity. Indeed, the yield was 98% for the first run and 84% for the 7th run. We conclude that low catalyst loading, operational simplicity, practicability and applicability to various substrates make this reaction an interesting alternative to previously applied procedures. From the environmental standpoint, this eco-friendly catalyst is stable, highly active, easy to prepare and handle.     

Vitamin B1 as a metal-free organocatalyst for greener Paal–Knorr pyrrole synthesis

This investigation discloses a greener reaction to prepare pyrrole derivatives. Metal-free catalysts are greener alternatives to existing metal catalysts in synthetic organic chemistry. Indeed, transition metals are often costly and toxic. They may be found as traces in health reaction products such as pharmaceuticals. Alternatively small organic molecules termed “organocatalysts” allow the synthesis of valuable products without traces of toxic metals. Here, we show for the first time the use of vitamin B₁ as new organocatalyst for the Paal–Knorr pyrrole synthesis under ambient conditions. Reaction conditions were optimized for the reaction of hexane-2,5-dione with 4-methoxyaniline. Ethanol was the most effective solvent. The conversion was quantitative using vitamin B₁, by comparison with a low yield of 30?% without catalysis. The best conditions were performed in ethanol with 5?mol % of vitamin B₁ during 1?h. This reaction was tested using various aromatic amines. To conclude the use of vitamin B₁ for the Paal–Knorr pyrrole, cyclocondensation has mild reaction conditions, is simple to perform, and gives moderate to excellent yields. It is therefore a promising reaction for the preparation of various pyrrole derivatives.     

Antiaflatoxigenic activity of Carum copticum essential oil

Plants are unique sources of useful metabolites. Plant essential oils display a wide range of antimicrobial effects against various pathogens. Here, we studied the essential oil from the seeds of Carum copticum. We monitored aflatoxin by high-performance liquid chromatography. Results show that Carum copticum essential oil inhibits Asergillus parasiticus growth and prevents aflatoxin production. The half-maximal inhibitory concentration (IC₅₀) is 127.5 μg mL^?1 for aflatoxin B₁ and 23.22 μg mL^?1 for aflatoxin G₁. Our findings show that Carum copticum essential oil is a potential candidate for the protection of foodstuff and feeds from toxigenic fungus growth and their subsequent aflatoxin contamination.     

Concentrations of Cd,Ni, Pb,and Cr in the two edible fish species Liza klunzingeri and Sillago sihama collected from Hara biosphere in Iran

The concentrations of four metals (Cd, Ni, Pb, and Cr) were determined in the muscles, gills, and livers of two edible fish species (Liza klunzingeri and Sillago sihama) caught from the Hara biosphere of Southern Iran. In both fish species, metal concentrations and bioaccumulation factors were in the sequence liver?>?gill?>?muscle. Bioaccumulation factors were found to be highest in S. sihama. The metal concentrations were descending in the order of Ni?>?Cr?>?Pb?>?Cd, except for muscle samples from S. sihama showing an inversion of Pb and Cr. There is a significant negative correlation between the concentrations of the metals in each tissue with length, weight, and age, except for muscle in L. klunzingeri. Some metal levels in the muscle exceeded the limits recommended by FAO, WHO, and FEPA.     

Synthesis and antibacterial activity of a Fe3O4–AgCl nanocomposite against Escherichia coli

In this investigation, Fe₃O₄ magnetic nanoparticles (MNPs) were prepared by the alkalinization of an aqueous medium containing ferrous sulfate and ferric chloride. In the next step, a Fe₃O₄–AgCl magnetic nanocomposite was fabricated by the drop-by-drop addition of silver nitrate solution into a NaCl solution containing Fe₃O₄ MNPs. All prepared nanoparticles were characterized by transition electron microscopy (TEM), X-ray diffraction (XRD), and energy-dispersive X-ray spectroscopy (EDS). Both particle types varied in size from 2.5 to 20?nm, with an average size of 7.5?nm for Fe₃O₄ MNPs and 12.5?nm for Fe₃O₄–AgCl nanocomposites. The antibacterial effect of the Fe₃O₄ MNPs and fabricated Fe₃O₄–AgCl nanocomposites against Escherichia coli (ATCC 35218) were investigated by conventional serial agar dilution method using the Müller–Hinton Agar medium. The minimum inhibitory concentration was 4?mg?mL^?1 for Fe₃O₄ MNPs and 2?mg?mL^?1 for the Fe₃O₄–AgCl magnetic nanocomposites. Time-kill course assays showed that the Fe₃O₄–AgCl magnetic nanocomposites successfully killed all inoculated bacterial cells during an exposure time of 60?min. The antibacterial activity of recycled Fe₃O₄–AgCl magnetic nanocomposites over four 60?min cycles of antibacterial treatment was further tested against E. coli by the colony-forming unit (CFU) method. The antibacterial efficiency of the nanocomposites was constant over two cycles of antibacterial testing.     

Bioremediation of toxic metals mercury and cesium using three types of biosorbent: bacterial exopolymer,gall nut,and oak fruit particles

Cesium and mercury are two mono-valent elements which can be found in toxic industrial, medical, and nuclear wastes. Their presence in the environment has deleterious effects on the ecosystem, living organisms including humans. Due to the chemical nature of these metals, bioremediation by conventional methods is more difficult to achieve compared to other metals. In this study, we used three biosorbents (oak powder, gall nut, and bacterial exopolymer) for the bioremediation of Hg and Cs. Bio-polymer was produced in the GMS mineral broth. Synthetic wastes of Hg(NO₃)₂ and isotope Cs-133 as the single-metal solutions were used. The biorefining process was carried out in glass columns, made of Pyrex, with dimensions 20?×?7/2?cm² with a V-shaped bottom. The samples were analyzed using atomic absorption. The experimental results showed that eliminated metal percent by oak powder, gall nut, and bacterial exopolymer were, respectively, of 94.8%, 96%, and 13.8% for Hg and 7.8%, 4.4%, and 69.4% for Cs. The tests revealed that Ca⁺⁺, when used as flocculant, played a key role in both biosorption and bio-precipitation rates. Consequently, it was concluded that the investigated biosorbents could be use as an integrated biosorption system for the refinement of mixed wastes.