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Sulfoxylates, formaldehyde

The reducing agents generally used in bleaching include sulfur dioxide, sulfurous acid, bisulfites, sulfites, hydrosulfites (dithionites), sodium sulfoxylate formaldehyde, and sodium borohydride. These materials are used mainly in pulp and textile bleaching (see Sulfur compounds Boron compounds). [Pg.149]

Sodium sulfoxylate formaldehyde, from Rohm and Haas. [Pg.196]

Zinc/organic acid Zinc sulfoxylate formaldehyde CATALYSTSL Eastern Color... [Pg.669]

Sodium sulfoxylate formaldehyde. See Sodium formaldehyde sulfor late... [Pg.1356]

Formaldehyde hydrosulfite. See Sodium formaldehyde sulfoxylate Formaldehyde methyl cyclododecyl acetal CAS 42604-12-6 EINECS/ELINCS 255-908-1 Synonyms Boisambrene Cyclododecane, (methoxymethoxy)- Formaldehyde cyclododecyl methyl acetal (Methoxymethoxy) cyclododecane Empincai C14H28O2 Properties M.w. 228.42 Toxicology LD50 (oral, rat) > 5 g/kg, (skin, rabbit) > 5 g/kg low toxicity by ing. and skin contact... [Pg.1843]

Formaldehyde sodium bisulfite adduct Formaldehyde sodium sulfoxylate. See Sodium formaldehyde sulfoxylate Formaldehyde o- and p-toluene sulfonamide. See Formaldehyde/toluenesulfonamide polymer... [Pg.1844]

Zinc fluorosilicate Zinc fluosilicate. See Zinc hexaf I uorosi I icate Zinc formaldehyde sulfoxylate CAS 24887-06-7 EINECS/ELINCS 246-515-6 Synonyms Bis (hydroxymethanesulfinato-0,0 ) zinc Zinc bis (hydroxymethanesulfinate) Zinc sulfoxylate formaldehyde Empirical C2H60eS2Zn Formula Zn(HS02 CH20)2 (normal) or Zn(0H)(HS02 CH2O) (basic)... [Pg.4752]

Zinc sulfocarbolate Zinc sulfophenate. See Zinc phenolsulfonate Zinc sulfoxylate formaldehyde. See Zinc formaldehyde sulfoxylate Zinc superoxide. See Zinc peroxide Zinc tallate... [Pg.4770]

The main advantages of post-polymerization treatments are that they can be carried out either in the polymerization reactor or in the storage tank, and no additional equipment is needed. However, only the polymerizable residual volatiles can be eliminated, and in some cases new VOCs are produced from secondary reactions. Thus, formaldehyde is formed when sodium sulfoxylate formaldehyde is used as the reductant [66] and acetone and fert-butanol are formed when tert-butyl hydroperoxide is used as the oxidant [67]. In addition, inorganic water-soluble initiators may be deleterious to both stability and water sensitivity of the film formed with the latexes. [Pg.981]

Fonnaldehyde hydrosulfite. See Sodium formaldehyde sulfoxylate Formaldehyde-naphthalenesulfonic acid copolymer. See Naphthalene-formaldehyde sulfonate... [Pg.2129]

Synonyms Disodium suiforicinoieate Uses Emulsifier and wetting agent Manuf./Distrib. Chemos GmbH Nanjing Chemlin Sodium sulfoxylate. See Sodium hydrosuifite Sodium sulfoxylate formaldehyde. See Sodium formaldehyde sulfoxylate Sodium tallamphopropionate CAS 68629-52-7 68991-88-8 EINECS/ELINCS 271-914-7 Synonyms 1-Hydroxyethyl-2-(tall oil) imidazoline-3-propanoic acid, inner salt Imi-dazolium compds., 1-(2-carboxyethyl)-4,5-dihydro-3-(hydroxyethyl)-2-nortall-oil alkyl, hydroxides, inner salts Tallamphopropionate Classification Amphoteric organic compd. [Pg.2459]

In addition to appHcations in dyeing, sodium formaldehyde sulfoxylate is used as a component of the redox system in emulsion polymerization of styrene—butadiene mbber recipes. [Pg.151]

Another hydrosulfite reducing agent is zinc formaldehyde sulfoxylate, Zn(HS02-CH20)2 (see Bleaching agents). [Pg.398]

Properties of zinc salts of inorganic and organic salts are Hsted in Table 1 with other commercially important zinc chemicals. In the dithiocarbamates, 2-mercaptobenzothiazole, and formaldehyde sulfoxylate, zinc is covalendy bound to sulfur. In compounds such as the oxide, borate, and sihcate, the covalent bonds with oxygen are very stable. Zinc—carbon bonds occur in diorganozinc compounds, eg, diethjizinc [557-20-0]. Such compounds were much used in organic synthesis prior to the development of the more convenient Grignard route (see Grignard reactions). [Pg.419]

Sodium formaldehyde sulfoxylate dihydrate (sodium hydroxymethylsulHnate, Rongalite)... [Pg.471]

In the presence of sodium bicarbonate, sodium formaldehyde sulfoxylate (Rongalite) converts perfluoroalkyl iodides and bromides to the corresponding carboxylates Less decarboxylation to the monohydroperfluoroalkanes occurs when the bromides are used [16] (equation 17)... [Pg.427]

About 20 grams of diamino diphenyl sulfone is dissolved in about 500 cc of ethyl alcohol (3A made up of 5 parts methyl alcohol and 100 parts of ethyl alcohol) by placing the ingredients in a flask provided with a reflux condenser and warming over a water bath. About 24 grams of pure grade, very finely powdered (40 to 60 mesh) sodium formaldehyde sulfoxylate Is then rapidly added to the alcohol solution of diamino diphenyl sulfone and the mixture refluxed in the usual manner. It was found that the mixture should be refluxed for a total of 5 hours and that a precipitate starts to form near the 3 hour period. The reaction mixture is then cooled to 15°C and kept at this temperature for about 1 hour. The precipitate formed in the filtrate is filtered off rapidly and drained as much as possible to remove mother liquor and then washed with small amounts of cold alcohol. The solid product is immediately placed in a desiccator and dried over sulfuric acid for about 20 hours. [Pg.1424]

Sodium formaldehyde sulfoxylates, 23 677 Sodium glucoheptonate, 4 708 Sodium D-gluconate, 4 708... [Pg.857]

Zinc formaldehyde sulfoxylates, 23 677 Zinc forming-die alloys, 26 594 Zinc foundry alloys, 26 591-594 Zinc hydrosulfite (dithionite), 26 559 Zinc hydroxypyridmethione biocide for antifouling coatings,... [Pg.1036]

Emulsion Polymerizations, eg. vinyl acetate [VAc]/ABDA, VAc/ethylene [VAE]/ABDA, butyl acrylate [BA]/ABDA, were done under nitrogen using mixed anionic/nonlonic or nonionic surfactant systems with a redox Initiator, eg. t-butyl hydroperoxide plus sodium formaldehyde sulfoxylate. Base monomer addition was batch or batch plus delay comonomer additions were delay. [Pg.470]

See other pages where Sulfoxylates, formaldehyde is mentioned: [Pg.910]    [Pg.149]    [Pg.149]    [Pg.910]    [Pg.517]    [Pg.1145]    [Pg.1346]    [Pg.4026]    [Pg.4636]    [Pg.455]    [Pg.2436]    [Pg.910]    [Pg.149]    [Pg.149]    [Pg.910]    [Pg.517]    [Pg.1145]    [Pg.1346]    [Pg.4026]    [Pg.4636]    [Pg.455]    [Pg.2436]    [Pg.904]    [Pg.1086]    [Pg.260]    [Pg.151]    [Pg.170]    [Pg.439]    [Pg.464]    [Pg.349]    [Pg.372]    [Pg.372]    [Pg.373]    [Pg.520]    [Pg.1424]    [Pg.338]    [Pg.471]    [Pg.151]   
See also in sourсe #XX -- [ Pg.132 , Pg.133 ]



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Formaldehyde-sulfoxylate

Formaldehyde-sulfoxylate acid, hydroxy

Sodium formaldehyde sulfoxylate

Sulfoxylates

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