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The heat of dilution can be defined from two perspectives: the differential heat and the integral heat. The differential heat of dilution is viewed on a micro scale, which is associated with the process in which a small amount of solvent is added to a large quantity of solution. The molar differential heat of dilution is thus defined as the enthalpy
Hydrogen peroxide is a chemical compound with the formula H 2 O 2.In its pure form, it is a very pale blue [5] liquid that is slightly more viscous than water.It is used as an oxidizer, bleaching agent, and antiseptic, usually as a dilute solution (3%–6% by weight) in water for consumer use and in higher concentrations for industrial use.
For example, 98% hydrogen peroxide is more stable than 70% hydrogen peroxide. Water acts as a contaminant, and the higher the water concentration the less stable the peroxide is. The storability of peroxide is dependent on the surface-to-volume ratio of the materials the fluid is in contact with.
Vaporized hydrogen peroxide (trademarked VHP, [1] also known as hydrogen peroxide vapor, HPV) is a vapor form of hydrogen peroxide (H 2 O 2) with applications as a low-temperature antimicrobial vapor used to decontaminate enclosed and sealed areas such as laboratory workstations, isolation and pass-through rooms, [2] and even aircraft interiors ...
Then, a catalyst, often around 10 ml potassium iodide solution or catalase from baker's yeast, is added to make the hydrogen peroxide decompose very quickly. Hydrogen peroxide breaks down into oxygen and water. As a small amount of hydrogen peroxide generates a large volume of oxygen, the oxygen quickly pushes out of the container. [6]
In the presence of a strong acid catalyst, such as sulfuric acid, acetic acid and hydrogen peroxide produce peracetic acid: [3] H 2 O 2 + CH 3 CO 2 H ⇌ CH 3 CO 3 H + H 2 O. However, in concentrations (3-6%) of vinegar and hydrogen peroxide marketed for household use, mixing without a strong acid catalyst will not form peracetic acid.
Diethyl ether hydroperoxide is the organic compound with the formula C 2 H 5 OCH(OOH)CH 3.It is a colorless liquid. Diethyl ether hydroperoxide and its condensation products are responsible for the explosive organic peroxides that slowly form upon exposure of diethyl ether to ambient air and temperature conditions.
The characteristic structure of any regular peroxide is the oxygen-oxygen covalent single bond, which connects the two main atoms together. In the event that the molecule has no chemical substituents, the peroxide group will have a [-2] net charge.