Flow Rate and Interference Studies for Copper Binding to a Silica-Immobilized Humin Polymer Matrix: Column and Batch Experiments

Batch and column experiments were performed to determine the Cu(II) binding capacity of silica-immobilized humin biomass. For column studies, 500 bed volumes of a 0.1 mM Cu(II) solution were passed through humin packed columns at the flow rates of 1, 1.5, 2, and 3 mL/min. The biopolymer showed an average Cu binding capacity of 12 ± 1.5 mg/g and a Cu recovery of about 96.5 % ± 1.5. The breakthrough points for Cu(II) alone were approximately 420, 390, 385, and 300 bed volumes for the flow rates of 1, 1.5, 2 and 3 mL/min, respectively. The interference studies demonstrated that at low concentrations, the hard cations Ca(II) and Mg(II) did not seem to represent a major interference on Cu(II) binding to the humin biopolymer. The selectivity showed by this biopolymer was Cu(II)>Ca(II)>Mg(II). On the other hand, batch experiments showed that Ca(II) + Mg(II) at 100mM each reduced the Cu(II) binding to 73 %. However, 1000 mM concentrations of Ca(II) and Mg(II), separately and in mixture, reduced the Cu(II) binding to 47 %, 44 % and 31 %, respectively. The results of this study showed that immobilized humin in a silica matrix could represent an inexpensive bio-source for Cu removal from contaminated water, even in the presence of low concentrations of the hard cations Ca(II) and Mg(II)

Sorption kinetic study of selenite and selenate onto a high and low pressure aged iron oxide nanomaterial

The sorption of selenite (SeO32−) and selenate (SeO42−) onto Fe3O4 nanomaterials produced by non microwave-assisted or microwave-assisted synthetic techniques was investigated through use of the batch technique. The phase of both synthetic nanomaterials was determined to be magnetite by X-ray diffraction. The average grain sizes of non microwave-assisted and microwave-assisted synthetic Fe3O4 were determined to be 27 and 25 nm, respectively through use of the Scherrer\u27s equation. Sorption of selenite was pH independent in the pH range of 2-6, while sorption of selenate decreased at pH 5 and 6. The addition of Cl− had no significant effect on selenite or selenate binding, while the addition of NO3− only affected selenate binding to the microwave assisted Fe3O4. A decrease of selenate binding to both synthetic particles was observed after the addition of SO42− while selenite binding was not affected. The addition of PO43− beginning at concentrations of 0.1 ppm had the most prominent effect on the binding of both selenite and selenate. The capacities of binding, determined through the use of Langmuir isotherm, were found to be 1923 and 1428 mg Se/kg of non microwave-assisted Fe3O4 and 2380 and 2369 mg Se/kg of microwave-assisted Fe3O4 for selenite and selenate, respectively

Do all Cu nanoparticles have similar applications in nano-enabled agriculture?

abstract: Copper-based chemicals have been widely used in agriculture as fertilizers and pesticides. Although these products have been essential to ensure food security, their continuous use has resulted in environmental pollution with detrimental effects for certain living organisms. Efforts have been put in place to reduce pollution derived from Cu application in agriculture. However, there is still a long way to go to reduce agrochemical applications without affecting food security. Copper-based nanomaterials including metallic copper (Cu NPs, nCu) copper oxide (CuO NPs, nCuO) and copper hydroxide [Cu(OH)2 nanowires, nCu(OH)2, Cu(OH)2 NPs] appear as the alternative to replace traditional copper-based agrochemicals. The available literature shows that the three nanomaterials have exhibited capabilities as nanofertilizers or nanopesticides. However, the data is very scattered and, in some cases, inconsistent. This minireview shows the most recent results from investigations about the effects of the three Cu-based nanomaterials in agricultural production. Advantages and disadvantages are discussed and research questions to guide future investigations are stated

Advanced Analytical Techniques for the Measurement of Nanomaterials in Food and Agricultural Samples

Nanotechnology offers substantial prospects for the development of state-of-the-art products and applications for agriculture, water treatment, and food industry. Profuse use of nanoproducts will bring potential benefits to farmers, the food industry, and consumers, equally. However, after end-user applications, these products and residues will find their way into the environment. Therefore, discharged nanomaterials (NMs) need to be identified and quantified to determine their ecotoxicity and the levels of exposure. Detection and characterization of NMs and their residues in the environment, particularly in food and agricultural products, have been limited, as no single technique or method is suitable to identify and quantify NMs. In this review, we have discussed the available literature concerning detection, characterization, and measurement techniques for NMs in food and agricultural matrices, which include chromatography, flow field fractionation, electron microscopy, light scattering, and autofluorescence techniques, among others

Removal of copper, lead, and zinc from contaminated water by saltbush biomass: Analysis of the optimum binding, stripping, and binding mechanism

Experiments performed on the Cu(II), Pb(II), and Zn(II) binding by saltbush biomass (Atriplex canescens) showed that the metal binding increased as pH increased from 2.0 to 5.0. The highest amounts of Cu, Pb, and Zn bound by the native biomass varied from 48-89%, 89-94%, and 65-73%, respectively. The hydrolyzed biomass bound similar amount of Pb and 50% more Cu and Zn than the native. The esterified biomass had a lower binding capacity than native; however, esterified flowers bound 45% more Cu at pH 2.0 than native flowers. The optimum binding time was 10 min or less. More than 60% of the bound Cu was recovered using 0.1 mM HCl, while more than 90% of Pb was recovered with either HCl or sodium citrate at 0.1 mM. For Zn, 0.1 mM sodium citrate allowed the recovery of 75%. Results indicated that carboxyl groups participate in the Cu, Pb, and Zn binding. © 2007

Effects of Copper Sulfate on Seedlings of Prosopis pubescens (Screwbean Mesquite)

Phytoextraction is an established method of removal of heavy metals from contaminated soils worldwide. Phytoextraction is most efficient if local plants are used in the contaminated site. We propose that Prosopis pubescens (Screw bean mesquite) would be a successful phytoextractor of copper in our local soils. In order to determine the feasibility of using Screw bean mesquite, we utilized inductively-coupled plasma-optical emission spectroscopy (ICP-OES) and elemental analysis to observe the uptake of copper and the effects on macro and micro nutrients within laboratory-grown seedlings. We have previously shown that P. pubescens is a hyperaccumulator of copper in soil-grown seedlings. Light and transmission electron microscopy demonstrated death of root cells and ultrastructural changes due to the presence of copper from 50 mg/L – 600 mg/L. Ultrastructural changes included plasmolysis, starch accumulation, increased vacuolation and swollen chloroplasts with disarranged thylakoid membranes in cotyledons. Inductively coupled plasma-optical emission spectroscopy analyses of macro- and micro-nutrients revealed that the presence of copper sulfate in the growth medium of Petri-dish grown Prosopis pubescens seedlings resulted in dramatic decreases of magnesium, potassium and phosphorus. At 500-600 mg/L of copper sulfate, a substantial increase of sulfur was present in roots