potassium-permanganate and ferrous-sulfate

The efficiency and mechanism of trace mercury (Hg(II)) removal by in situ formed manganese-ferric (hydr)oxides (in situ Mn-Fe) were investigated by reacting KMnO4 with Fe(II) in simulated solutions and natural water. In the simulated solutions, the impact of coagulant dosage, pH, and temperature on mercury removal was studied. Experimental results showed that in situ Mn-Fe more effectively removed mercury compared with polyaluminum chloride (PAC) and iron(III) chloride (FeCl3), and that mercury existed in the form of uncharged species, namely Hg(OH)2, HgClOH(aq), and HgCl2(aq). Fourier transform infrared spectroscopy demonstrated that in situ Mn-Fe contained hydroxyl groups as the surface active sites, while X-ray photoelectron spectroscopy (XPS) measurements revealed that MnO2 or MnOOH and FeOOH were the dominant species in the precipitates. XPS analysis indicated that an Hg-Mn-Fe mixture was formed in the precipitates, suggesting that mercury was removed from solutions via transfer from the liquid phase to solid phase. These results indicated that the primary mercury removal mechanisms in in situ Mn-Fe were surface complexation and flocculation-precipitation processes. Satisfactory removal efficiency of mercury was also observed following in situ Mn-Fe in natural waters.

Topics: Aluminum Hydroxide; Chlorides; Ferric Compounds; Ferrous Compounds; Mercury; Photoelectron Spectroscopy; Potassium Permanganate; Spectroscopy, Fourier Transform Infrared; Water Pollutants, Chemical

This paper reports the results of an experimental study testing a low-cost in situ chemical fixation method designed to reclaim arsenic-contaminated subsurface soils. Subsurface soils from several industrial sites in southeastern U.S. were contaminated with arsenic through heavy application of herbicide containing arsenic trioxide. The mean concentrations of environmentally available arsenic in soils collected from the two study sites, FW and BH, are 325 mg/kg and 900 mg/kg, respectively. The soils are sandy loams with varying mineralogical and organic contents. The previous study [Yang L, Donahoe RJ. The form, distribution and mobility of arsenic in soils contaminated by arsenic trioxide, at sites in Southeast USA. Appl Geochem 2007;22:320-341] indicated that a large portion of the arsenic in both soils is associated with amorphous aluminum and iron oxyhydroxides and shows very slow release against leaching by synthetic precipitation. The soil's amorphous aluminum and iron oxyhydroxides content was found to have the most significant effect on its ability to retain arsenic. Based on this observation, contaminated soils were reacted with different treatment solutions in an effort to promote the formation of insoluble arsenic-bearing phases and thereby decrease the leachability of arsenic. Ferrous sulfate, potassium permanganate and calcium carbonate were used as the reagents for the chemical fixation solutions evaluated in three sets of batch experiments: (1) FeSO(4); (2) FeSO(4) and KMnO(4); (3) FeSO(4), KMnO(4) and CaCO(3). The optimum treatment solutions for each soil were identified based on the mobility of arsenic during sequential leaching of treated and untreated soils using the fluids described in EPA Method 1311 [USEPA. Method 1311: toxicity characteristic leaching procedure. Test methods for evaluating solid waste, physical/chemical methods. 3rd ed. Washington, DC: U.S. Environmental Protection Agency, Office of Solid Waste. U.S. Government Printing Office; 1992] toxic characteristics leaching procedure (TCLP) and EPA Method 1312 [USEPA. Method 1312: synthetic precipitation leaching procedure. Test methods for evaluating solid waste, physical/chemical methods. 3rd ed. Washington, DC: U.S. Environmental Protection Agency, Office of Solid Waste. U.S. Government Printing Office; 1994] synthetic precipitation leaching procedure (SPLP). Both FW and BH soils showed significant decreases in arsenic leachability for all three treatment solutions, compare

Topics: Arsenic; Calcium Carbonate; Chemical Fractionation; Ferrous Compounds; Industrial Waste; Potassium Permanganate; Soil Pollutants; Waste Management

The effects of 6 different litter amendments on broiler performance, level of atmospheric ammonia (NH3) concentration, and soluble reactive phosphorus (SRP) in litter was determined. Through 3 experiments conducted on 2 different commercial farms, one chemical amendment was added to the litter and then was compared with a control. Broiler performance was not affected by any of the amendments except the ferrous sulfate amendment for which mortality was 25.5%. Application of aluminum chloride (AlCl3 x 6H2O) to the litter lowered atmospheric ammonia concentrations at 42 d by 97.2%, whereas ferrous sulfate (FeSO4 x 7H2O) lowered it by 90.77%. Ammonia concentrations were reduced by 86.18, 78.66, 75.52, and 69.00% by aluminum sulfate [alum or Al2(SO4)3 x 14H2O)], alum + CaCO3, aluminum chloride + CaCO3, and potassium permanganate (KMnO4), respectively, when compared with each control at 42 d. Each amendment except KMnO4 significantly reduced SRP contents. Alum and aluminum chloride were the effective compounds evaluated on the commercial farms with respect to reducing ammonia contents, phosphorus solubility, and mortality.

Topics: Air Pollution; Alum Compounds; Aluminum Chloride; Aluminum Compounds; Ammonia; Animal Husbandry; Animals; Calcium Carbonate; Chickens; Chlorides; Ferrous Compounds; Housing, Animal; Phosphorus; Potassium Permanganate; Time Factors

In Xer site-specific recombination, two related recombinases, XerC and XerD, mediate the formation of recombinant products using Holliday junction-containing DNA molecules as reaction intermediates. Each recombinase catalyses the exchange of one pair of specific strands. By using synthetic Holliday junction-containing recombination substrates in which two of the four arms are tethered in an antiparallel configuration by a nine thymine oligonucleotide, we show that XerD catalyses efficient strand exchange only when its substrate strands are 'crossed'. XerC also catalyses very efficient strand exchange when its substrate strands are 'crossed', though it also appears to be able to mediate strand exchange when its substrate strands are 'continuous'. By using chemical probes of Holliday junction structure in the presence and absence of bound recombinases, we show that recombinase binding induces unstacking of the bases in the centre of the recombination site, indicating that the junction branch point is positioned there and is distorted as a consequence of recombinase binding.

Topics: Bacterial Proteins; Binding Sites; Catalysis; Deoxyribonuclease BamHI; Deoxyribonucleases, Type II Site-Specific; DNA Nucleotidyltransferases; DNA, Bacterial; Edetic Acid; Escherichia coli; Escherichia coli Proteins; Ferrous Compounds; Hydroxyl Radical; Integrases; Nucleic Acid Conformation; Osmium Tetroxide; Oxidants; Potassium Permanganate; Proteins; Recombinases; Substrate Specificity; Thymine

Topics: Coronary Disease; Ferrous Compounds; Free Radicals; Humans; Lipids; Methods; Oxidation-Reduction; Peroxides; Potassium Permanganate