Jason G. Parsons

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

The sorption of selenite (SeO(3)(2-)) and selenate (SeO(4)(2-)) onto Fe(3)O(4) 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 Fe(3)O(4) were determined to be 27 and 25 nm, respectively through use of the Scherrers 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 NO(3)(-) only affected selenate binding to the microwave assisted Fe(3)O(4). A decrease of selenate binding to both synthetic particles was observed after the addition of SO(4)(2-) while selenite binding was not affected. The addition of PO(4)(3-) 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 Fe(3)O(4) and 2380 and 2369 mg Se/kg of microwave-assisted Fe(3)O(4) for selenite and selenate, respectively.

Study of the thermodynamics of chromium(III) and chromium(VI) binding to iron(II/III)oxide or magnetite or ferrite and magnanese(II) iron (III) oxide or jacobsite or manganese ferrite nanoparticles.

Removal of chromium(III) or (VI) from aqueous solution was achieved using Fe3O4, and MnFe2O4 nanomaterials. The nanomaterials were synthesized using a precipitation method and characterized using XRD. The size of the nanomaterials was determined to be 22.4±0.9 nm (Fe3O4) and 15.5±0.5 nm (MnFe2O4). The optimal binding pH for chromium(III) and chromium(VI) were pH 6 and pH 3. Isotherm studies were performed, under light and dark conditions, to determine the capacity of the nanomaterials. The capacities for the light studies with MnFe2O4 and Fe3O4 were determined to be 7.189 and 10.63 mg/g, respectively, for chromium(III). The capacities for the light studies with MnFe2O4 and Fe3O4 were 3.21 and 3.46 mg/g, respectively, for chromium(VI). Under dark reaction conditions the binding of chromium(III) to the MnFe2O4 and Fe3O4 nanomaterials were 5.74 and 15.9 mg/g, respectively. The binding capacity for the binding of chromium(VI) to MnFe2O4 and Fe3O4 under dark reaction conditions were 3.87 and 8.54 mg/g, respectively. The thermodynamics for the reactions showed negative ΔG values, and positive ΔH values. The ΔS values were positive for the binding of chromium(III) and for chromium(VI) binding under dark reaction conditions. The ΔS values for chromium(VI) binding under the light reaction conditions were determined to be negative.

Prepubertal exposure to arsenic(III) suppresses circulating insulin-like growth factor-1 (IGF-1) delaying sexual maturation in female rats

Arsenic (As) is a prevalent environmental toxin readily accessible for human consumption and has been identified as an endocrine disruptor. However, it is not known what impact As has on female sexual maturation. Therefore, in the present study, we investigated the effects of prepubertal exposure on mammary gland development and pubertal onset in female rats. Results showed that prepubertal exposure to 10 mg/kg of arsenite (As(III)) delayed vaginal opening (VO) and prepubertal mammary gland maturation. We determined that As accumulates in the liver, disrupts hepatocyte function and suppresses serum levels of the puberty related hormone insulin-like growth factor 1 (IGF-1) in prepubertal animals. Overall, this is the first study to show that prepubertal exposure to As(III) acts peripherally to suppress circulating levels of IGF-1 resulting in delayed sexual maturation. Furthermore, this study identifies a critical window of increased susceptibility to As(III) that may have a lasting impact on female reproductive function.

ADSORPTION OF SELENITE AND SELENATE BY A HIGH- AND LOW-PRESSURE AGED MANGANESE OXIDE NANOMATERIAL

This study investigated the effects of pH, reaction time, competitive anions, and adsorption capacity through the use of Langmuir isotherms of selenite and selenate binding to engineered Mn3O4 nanomaterials aged using two different techniques through use of dynamic reaction cell inductively coupled plasma–mass spectrometry (DRC-ICP-MS). The phases and average grain sizes of the synthesized materials were determined through x-ray diffraction and Scherrers equation. The optimal binding occurred at pH 4 within 10 min of contact time for both materials. The addition of Cl−, , and all decreased selenate binding, while only decreased selenite binding. The binding capacities were found to be 507 and 800 mg Se/kg of non-microwave-assisted Mn3O4 for selenite and selenate, respectively. The microwave-assisted Mn3O4 displayed binding capacities of 1000 and 934.5 mg Se/kg of nanomaterial for selenite and selenate, respectively.

SPECTROSCOPIC DETERMINATION OF THE TOXICITY, ABSORPTION, REDUCTION, AND TRANSLOCATION OF Cr(VI) IN TWO MAGNOLIOPSIDA SPECIES

Hexavalent chromium is a contaminant highly mobile in the environment that is toxic for plants at low concentrations. In this work, the physiological response of Convolvulus arvensis and Medicago truncatula plants to Cr(VI) treatments was compared. C. arvensis is a potential Cr hyperaccumulator well adapted to semiarid conditions that biotransform Cr(VI) to the less toxic Cr(III). M. truncatula is a model plant well adapted to semiarid conditions with a well studied genetic response to heavy metal stress. The results demonstrated that C. arvensis is more tolerant to Cr toxicity and has a higher Cr translocation to the leaves. The inductively coupled plasma optical emission spectroscopy results showed that C. arvensis plants treated with 10 mg Cr(VI) L–1 accumulated 1512, 210, and 131 mg Cr kg–1 in roots, stems, and leaves, respectively. While M. truncatula plants treated with the same Cr(VI) concentration accumulated 1081, 331, and 44 (mg Cr kg–1) in roots, stems, and leaves, respectively. Enzymatic assays demonstrated that Cr(VI) decreased ascorbate peroxidase activity and increased catalase activity in M. truncatula, while an opposite response was found in C. arvensis. The x-ray absorption spectroscopy studies showed that both plant species reduced Cr(VI) to the less toxic Cr(III).

Thermodynamic and kinetic study of the removal of Cu 2+ and Pb 2+ ions from aqueous solution using Fe 7 S 8 nanomaterial

In the present study, pyrrhotite (Fe7S8) was investigated for the removal of Pb2+ and Cu2+ ions from aqueous solution. The Fe7S8 material was prepared through a solvothermal method and was characterized using XRD. The average particle size for the nanomaterial was determined to be 29.86 ± 0.87 nm using XRD analysis and Scherrers equation. Batch studies were performed to investigate the effects of pH, time, temperature, interfering ions, and the binding capacity of Pb2+ and Cu2+ ions to the Fe7S8 nanomaterial. During the pH profile studies, the optimum pH for the binding of Pb2+ and Cu2+ was determined to be pH 5 for both cations. Isotherm studies were conducted from which the thermodynamics and binding capacities for both Cu2+ and Pb2+ were determined. The binding capacity for Pb2+ and Cu2+ binding to the Fe7S8 were determined to be 0.039 and 0.102 mmol/g, respectively at 25°C. The thermodynamic parameters indicated a ΔG for the sorption of Pb2+ ranged from 5.07 kJ/mol to -2.45 kJ/mol indicating a non-spontaneous process was occurring. Whereas, the ΔG for Cu2+ ion binding ranged from 9.78 kJ/mol to -11.23 kJ/mol indicating a spontaneous process at higher temperatures. The enthalpy indicated an endothermic reaction was occurring for the binding of Pb2+ and Cu2+ to the Fe7S8 nanomaterial with ΔH values of 55.8 kJ/mol and 153.5 kJ/mol, respectively. Furthermore, the ΔS values for the reactions were positive indicating an increase in the entropy of the system after metal ion binding. Activation energy studies indicated the binding for both Pb2+ and Cu2+ occurred through chemisorption.