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The Marsh test treats the sample with sulfuric acid and arsenic-free zinc. Even if there are minute amounts of arsenic present, the zinc reduces the trivalent arsenic (As 3+). Here are the two half-reactions: Oxidation: Zn → Zn 2+ + 2 e − Reduction: As 2 O 3 + 12 e − + 6 H + → 2 As 3− + 3 H 2 O. Overall, we have this reaction:
In the Gutzeit test, AsH 3 is generated by reduction of aqueous arsenic compounds, typically arsenites, with Zn in the presence of H 2 SO 4. The evolved gaseous AsH 3 is then exposed to AgNO 3 either as powder or as a solution. With solid AgNO 3, AsH 3 reacts to produce yellow Ag 4 AsNO 3, whereas AsH 3 reacts with a solution of AgNO 3 to give ...
Like all arsenic-containing compounds, arsonic acids are toxic and carcinogenic to humans. [1] [2] Arsonic acid refers to H 3 As O 3, the case where the substituent is a single hydrogen atom. The other arsonic acids can simply be viewed as hydrocarbyl derivatives of this base case. Arsenic acid results when the substituent is a hydroxyl group.
The behaviour of the coal's ash residue at high temperature is a critical factor in selecting coals for steam power generation. Most furnaces are designed to remove ash as a powdery residue. Coal which has ash that fuses into a hard glassy slag known as clinker is usually unsatisfactory in furnaces as it requires cleaning. However, furnaces can ...
At the level of the citric acid cycle, arsenic inhibits lipoic acid, which is a cofactor for pyruvate dehydrogenase. By competing with phosphate, arsenate uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration and ATP synthesis. Hydrogen peroxide production is also increased, which, it is ...
Arsenic acid or arsoric acid is the chemical compound with the formula H 3 AsO 4. More descriptively written as AsO(OH) 3, this colorless acid is the arsenic analogue of phosphoric acid. Arsenate and phosphate salts behave very similarly. Arsenic acid as such has not been isolated, but is only found in solution, where it is largely ionized.
Cacodylic acid, central to arsenic chemistry, arises from the methylation of arsenic(III) oxide. (In contrast, the dimethylphosphonic acid is less significant in the corresponding chemistry of phosphorus.) Phenylarsonic acids can be accessed by the reaction of arsenic acid with anilines, the so-called Bechamp reaction.
Arsonic acid is the simplest of the arsonic acids. It is a hypothetical compound , although the tautomeric arsenious acid (As(OH) 3 ) is well established. In contrast to the instability of HAsO(OH) 2 , the phosphorus compound with analogous stoichiometry exists as the tetrahedral tautomer.