Valence State Of Arsenic Research Articles

Elimination of Arsenic (III) using Phaseolus Lunatus and Phaseolus Vulgaris as Natural Coagulants

In this analysis, the efficacy of adding coagulants such as Phaseolus lunatus and Phaseolus vulgaris (polymers) to the coagulation process during the treatment of arsenic aqueous solution to extract the arsenic metal was investigated. Experiments were carried out to evaluate the output of Phaseolus lunatus and Phaseolus vulgaris, both individually and in combination with arsenic, using the standard Jar test protocol. P.lunatus and P.vulgaris were given doses ranging from 1 to 3 gm. For P.lunatus and P.vulgaris, the (optimal) removal efficiency for total arsenic in the aqueous solution was obtained at 2gm. With chemical affinity between arsenic and coagulants used in this process, the valence state of arsenic may affect removal efficiency during the chemical coagulation process. pH is discovered to be a significant factor that has a direct or indirect impact on results. By overcoming the isoelectric point, the complex formed by the interaction of the inorganic pollutant and organic coagulant may aid in the removal of arsenic at pH 9 and 8. P.lunatus and P.vulgaris had optimised arsenic initial concentrations of 57.1µg/L and 42.6µg/L, respectively. The coagulation mechanism is more prevalent in water treatment, as shown by the above findings.

Physicochemical and environmental properties of arsenic sulfide sludge from copper and lead−zinc smelter

Abstract Physicochemical properties of arsenic sulfide sludge (ASS) from copper smelter (ASS-I) and lead−zinc smelter (ASS-II) were examined by XRD, Raman spectroscopy, SEM−EDS, TG−DTA, XPS and chemical phase analysis method. The toxicity characteristic leaching procedure (TCLP), Chinese standard leaching tests (CSLT), three-stage sequential extraction procedure (BCR) and batch leaching experiments (BLE) were used to investigate the environmental stability. The ASSs from different smelters had obviously different physicochemical and environmental properties. The phase composition and micrograph analysis indicate that ASS-I mainly consists of super refined flocculent particles including amorphous arsenic sulfide adhered with amorphous sulfur and that ASS-II mainly consists of amorphous arsenic sulfide. The valence state of arsenic in both sludges is trivalent, but the valence composition of sulfur is quite different. The ASSs have thermal instability properties. The results of TCLP and CSLT indicate that the concentrations of As and Pd in the leaching solution exceed the standard limits. More than 5% and 90% of arsenic are in the form of acid soluble and oxidizable fractions, respectively, which explains the high arsenic leaching toxicity and environmental activity of ASS. This research provides comprehensive information for the disposal of ASS from copper and lead−zinc smelter.

Acute toxicity of arsenic to larvae of four New Zealand freshwater insect taxa

ABSTRACTArsenic, often found in gold deposits, can enter aquatic systems. The toxicity of arsenate (As(V)), the most common valence state of arsenic in freshwater, was assessed on the larvae of four freshwater insect taxa from naturally acidic (pH 5.9) and circumneutral (pH 7.4) New Zealand streams. Insects from the acidic stream were more sensitive to arsenate-spiked water than those from the circumneutral stream. Early instars (<3 mm) of the mayfly Deleatidium spp. (Leptophlebiidae) were the most sensitive compared to later instars (3–6 mm) (4-d LC50 1.5 and 3.5 mg/L, respectively) or to the stonefly Zelandobius spp. (Gripopterygidae) (4-d LC50 2.5 mg/L). The cased caddisflies Pycnocentria spp. (Conoesucidae) and Helicopsyche spp. (Helicopsychidae) from circumneutral stream were the most tolerant (4-d LC50 45.4 and 113 mg/L, respectively). The 14-day arsenic LC10 and LC50 for Deleatidium spp. late instars exposed to mining-impacted water were 0.12 and 0.36 mg/L, respectively.

Rapid Equilibrium Kinetic Analysis of Arsenite Methylation Catalyzed by Recombinant Human Arsenic (+3 Oxidation State) Methyltransferase (hAS3MT)

In the human body, arsenic is metabolized by methylation. Understanding this process is important and provides insight into the relationship between arsenic and its related diseases. We used the rapid equilibrium kinetic model to study the reaction sequence of arsenite methylation. The results suggest that the mechanism for arsenite methylation is a completely ordered mechanism that is also of general interest in reaction systems with different reductants, such as tris(2-carboxyethyl)phosphine, cysteine, and glutathione. In the reaction, cysteine residues of recombinant human arsenic (+3 oxidation state) methyltransferase (hAS3MT) coordinate with arsenicals and involve the methyl transfer step. S-Adenosyl-l-methionine (AdoMet) is the first-order reactant, which modulates the conformation of hAS3MT to a best matched state by hydrophobic interaction. As the second-order reactant, reductant reduces the disulfide bond, most likely between Cys-250 and another cysteine residue of hAS3MT, and exposes the active site cysteine residues for binding trivalent inorganic arsenic (iAs(3+)) to give monomethylarsonic dicysteine (MADC(3+)). In addition, the reaction can be extended to further methylate MADC(3+) to dimethylarsinic cysteine (DAMC(3+)). In the methylation reaction, the β-pleated sheet content of hAS3MT is increased, and the hydrophobicity of the microenvironment around the active sites is decreased. Similarly, we confirm that both the high β-pleated sheet content of hAS3MT and the high dissociation ability of the enzyme-AdoMet-reductant improve the yield of dimethylated arsenicals.

Characteristics of arsenic accumulation by the seaweeds Fucus spiralis and Ascophyllum nodosum

This study examines the accumulation of 74As-arsenic in the seaweeds Fucus spiralis (L.) and Ascophyllum nodosum (L.) collected from Restronguet Creek in southwest England during 1978. Also, the influence of environmental factors (valence state of arsenic, pH, salinity, temperature, phosphate concentration) and metabolic inhibitors on the uptake of arsenic by F. spiralis is examined. Most of the arsenic in the seaweeds was non-exchangeable with labelled arsenic in the medium. The accumulation of 74As reached a steady state in 1 to 8 d, depending on the species and external arsenic concentration. At steady state the accumulated arsenic is proportional to external arsenate concentration. F. spiralis accumulated 4 times more arsenate than arsenite. The short-term uptake of arsenic increased in proportion to the external arsenic concentration up to a level of 1000 μg l-1; it then remained constant at higher levels of arsenic. Arsenic uptake increased in direct proportion to increasing temperature. Variation of pH or salinity had no effect on arsenic incorporation. The accumulation of arsenic occurred only in living tissue and was inhibited by KCN in a concentration-dependent manner. The uptake of arsenic by F. spiralis in the presence of photo-synthetic inhibitors (DCMU or CMU) or in the dark was greater than in the light controls. Thus, it was concluded that energy is required for arsenic uptake and this is derived from respiration rather than photosynthesis. There was no evidence for a common mechanism of phosphate and arsenate uptake by macroalgae, although high concentrations of phosphate (40 to 400 μM) initially inhibited arsenate uptake.