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Peroxide-based Bleach
A peroxide-based bleach or simply peroxide bleach is any bleach product that is based on the peroxide chemical group, namely two oxygen atoms connected by a single bond, (–O–O–). This bond is fairly weak and is often broken in chemical reactions of peroxides, giving rise to very reactive oxygen species, which are the active agents of the bleach. Peroxide-based bleaches became common household products in the late 20th century, being the base of many laundry detergent formulations. Most of these products are adducts of hydrogen peroxide ( or ), that is, solids that contain trapped in a crystal structure together with another material like sodium carbonate or urea. An exception is sodium perborate, which has a cyclic structure containing two O-O single bonds. Peroxide bleaches are considered to be eco-friendly cleaning agents, compared to chlorine-based bleaches that might produce organochlorine compounds. Chemistry All peroxide-based bleaches release hydrogen peroxide w ...
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Bleach
Bleach is the generic name for any chemical product that is used industrially or domestically to remove color from (i.e. to whiten) fabric or fiber (in a process called bleaching) or to disinfect after cleaning. It often refers specifically to a dilute solution of sodium hypochlorite, also called "liquid bleach". Many bleaches have broad-spectrum bactericidal properties, making them useful for disinfecting and sterilizing. They are used in swimming pool sanitation to control bacteria, viruses, and algae and in many places where sterile conditions are required. They are also used in many industrial processes, notably in the bleaching of wood pulp. Bleaches also have other minor uses, like removing mildew, killing weeds, and increasing the longevity of cut flowers. Bleaches work by reacting with many colored organic compounds, such as natural pigments, and turning them into colorless ones. While most bleaches are oxidizing agents (chemicals that can remove electrons from ot ...
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Bleach Activator
Bleach activators are compounds that allow a lower washing temperature than would be required otherwise to achieve the full activity of bleaching agents in the wash liquor. Bleaching agents, usually peroxides, are usually sufficiently active only from 60 °C on. With bleach activators, this activity can already be achieved at lower temperatures. Bleach activators react with hydrogen peroxide in aqueous solution to form peroxy acids. Peroxy acids are more active bleaches than hydrogen peroxide at lower temperatures (<60 °C) but are too unstable to be stored in their active form and hence must be generated in situ. The most common bleach activators used commercially are tetraacetylethylenediamine (TAED) and sodium nonanoyloxybe ...
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Peroxides
In chemistry, peroxides are a group of compounds with the structure , where the R's represent a radical (a portion of a complete molecule; not necessarily a free radical) and O's are single oxygen atoms. Oxygen atoms are joined to each other and to adjacent elements through single covalent bonds, denoted by dashes or lines. The group in a peroxide is often called the peroxide group, though some nomenclature discrepancies exist. This linkage is recognized as a common polyatomic ion, and exists in many molecules. General structure 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. Each oxygen atom has a charge of negative one, as 5 of its valence electrons remain in the outermost orbital shell whilst one is occupied in the covalent bond. Because of the nature of the covalent bo ...
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Ozone
Ozone () (or trioxygen) is an Inorganic compound, inorganic molecule with the chemical formula . It is a pale blue gas with a distinctively pungent smell. It is an allotrope of oxygen that is much less stable than the diatomic allotrope , breaking down in the lower atmosphere to (dioxygen). Ozone is formed from dioxygen by the action of ultraviolet (UV) light and electrical discharges within the Earth's atmosphere. It is present in very low concentrations throughout the atmosphere, with its highest concentration high in the ozone layer of the stratosphere, which absorbs most of the Sun's ultraviolet (UV) radiation. Ozone's odor is reminiscent of chlorine, and detectable by many people at concentrations of as little as in air. Ozone's O3 chemical structure, structure was determined in 1865. The molecule was later proven to have a bent structure and to be weakly diamagnetism, diamagnetic. At standard temperature and pressure, ozone is a pale blue gas that condenses at cryogenic ...
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Chlorine-based Bleach
Chlorine-releasing compounds, also known as chlorine base compounds, is jargon to describe certain chlorine-containing substances that are used as disinfectants and bleaches. They include the following chemicals: sodium hypochlorite (active agent in bleach), chloramine, halazone, and sodium dichloroisocyanurate. They are widely used to disinfect water and medical equipment, and surface areas as well as bleaching materials such as cloth. The presence of organic matter can make them less effective as disinfectants. They come as a liquid solution, or as a powder that is mixed with water before use. Side effects if contact occurs may include skin irritation and chemical burns to the eye. They may also cause corrosion and therefore may require being rinsed off. Specific compounds in this family include sodium hypochlorite, monochloramine, halazone, chlorine dioxide, and sodium dichloroisocyanurate. They are effective against a wide variety of microorganisms including bacterial ...
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Nucleophile
In chemistry, a nucleophile is a chemical species that forms bonds by donating an electron pair. All molecules and ions with a free pair of electrons or at least one pi bond can act as nucleophiles. Because nucleophiles donate electrons, they are Lewis bases. ''Nucleophilic'' describes the affinity of a nucleophile to bond with positively charged Atomic nucleus, atomic nuclei. Nucleophilicity, sometimes referred to as nucleophile strength, refers to a substance's nucleophilic character and is often used to compare the affinity of atoms. Neutral nucleophilic reactions with solvents such as Alcohol (chemistry), alcohols and water are named solvolysis. Nucleophiles may take part in nucleophilic substitution, whereby a nucleophile becomes attracted to a full or partial positive charge, and nucleophilic addition. Nucleophilicity is closely related to basicity. The difference between the two is, that basicity is a thermodynamic property (i.e. relates to an equilibrium state), but nucleop ...
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Sodium Perborate
Sodium perborate are chemical compounds with chemical formula (H2O)x. Commonly encountered salts are the anhydrous form (x = 0) and as a hydrate, hexahydrate (x = 6). These two species are sometimes called, respectively, "monohydrate" or PBS-1 and "tetrahydrate" or PBS-4, after the historic assumption that would be the anhydrous form). Both the anhydrous and hexahydrate salts are white, odorless, water-soluble solids. Peroxyborates are widely used in laundry detergents, as one of the peroxide-based bleaches. Sodium perborate was first obtained in 1898, independently, by Sebastian Tanatar and by P. Melikoff and L. Pissadewsky; the researchers prepared sodium perborate by treating sodium borate with a solution of hydrogen peroxide and sodium hydroxide, but Tanatar also obtained sodium perborate by electrolysis of a solution of sodium borate. Structure Unlike sodium percarbonate, the peroxyborates are not adducts of hydrogen peroxide. Rather, they contain a peroxyborate anion , ...
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Saponification
Saponification is a process of cleaving esters into carboxylate salts and Alcohol (chemistry), alcohols by the action of aqueous alkali. Typically aqueous sodium hydroxide solutions are used. It is an important type of alkaline hydrolysis. When the carboxylate is long chain, its salt is called a soap. The saponification of ethyl acetate gives sodium acetate and ethanol: : Saponification of fats Vegetable oils and animal fats are the traditional materials that are saponified. These greasy materials, triesters called triglycerides, are usually mixtures derived from diverse fatty acids. In the traditional saponification, the triglyceride is treated with lye, which cleaves the ester bonds, releasing fatty acid salts (soaps) and glycerol. In one simplified version, the saponification of stearin gives sodium stearate. : This process is the main industrial method for producing glycerol (). Some soap-makers leave the glycerol in the soap. Others precipitation (chemistry), precipitate t ...
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Sodium Percarbonate
Sodium percarbonate or sodium carbonate peroxide is an inorganic compound with the formula . It is an adduct of sodium carbonate ("soda ash" or "washing soda") and hydrogen peroxide (that is, a perhydrate). It is a colorless, crystalline, hygroscopic, and water-soluble solid. It is sometimes abbreviated as SPC. It contains 32.5% by weight of hydrogen peroxide. The product is used in some eco-friendly bleaches and other cleaning products. History Sodium percarbonate was first prepared in 1899 by Ukrainian chemist Sebastian Moiseevich Tanatar (7 October 1849 – 30 November 1917). Structure At room temperature, solid sodium percarbonate has the orthorhombic crystal structure, with the ''Cmca'' crystallographic space group. The structure changes to ''Pbca'' as the crystals are cooled below about −30 °C. Chemistry Dissolved in water, sodium percarbonate yields a mixture of hydrogen peroxide, sodium cations (), and carbonate (). : Production Sodium percarbonate is p ...
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Hydrogen Peroxide
Hydrogen peroxide is a chemical compound with the formula . In its pure form, it is a very pale blue liquid that is slightly more viscosity, viscous than Properties of water, 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. Concentrated hydrogen peroxide, or "high-test peroxide", decomposes explosively when heated and has been used as both a monopropellant and an oxidizer in rocketry. Hydrogen peroxide is a reactive oxygen species and the simplest peroxide, a compound having an oxygen–oxygen single bond. It decomposes slowly into water and elemental oxygen when exposed to light, and rapidly in the presence of organic or reactive compounds. It is typically stored with a Stabilizer (chemistry), stabilizer in a weakly acidic solution in an opaque bottle. Hydrogen peroxide is found in biological systems including the human body. Enzymes that u ...
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Sodium Nonanoyloxybenzenesulfonate
Sodium nonanoyloxybenzenesulfonate (NOBS) is an important component of laundry detergents and bleaches. It is known as a bleach activator for active oxygen sources, allowing formulas containing hydrogen peroxide releasing chemicals (specifically sodium perborate, sodium percarbonate, sodium perphosphate, sodium persulfate, and urea peroxide) to effect bleaching at lower temperatures. Synthesis NOBS is formed by the reaction of nonanoic acid (or its esters) with phenol followed by aromatic sulfonation using SO3 to form a sulfonic acid at the para-position. Bleach activation NOBS was developed by Procter & Gamble The Procter & Gamble Company (P&G) is an American multinational consumer goods corporation headquartered in Cincinnati, Ohio. It was founded in 1837 by William Procter and James Gamble. It specializes in a wide range of personal health/con ... in 1983 and was first used in American laundry detergents in 1988. NOBS is the main bleach activator used in the U ...
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