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Amines triethanolamine

Persulfate (41) reacts with transition metal ions (e.g. Ag, Fe21, Ti31) according to Scheme 3.42. Various other reduetants have been described. These include halide ions, thiols (e.g. 2-mercaptoethanol, thioglycolic acid, cysteine, thiourea), bisulfite, thiosulfate, amines (triethanolamine, tetramethylethylenediamine, hydrazine hydrate), ascorbic acid, and solvated electrons (e.g. in radiolysis). The mechanisms and the initiating species produced have not been fully elucidated for... [Pg.95]

All these compounds are organosilicon ethers of biogenic amines (triethanolamine, diethylamine) or diethylene glycol. But we failed to obtain similar atrane derivatives of glycerin. At the same time we obtained and described for the first time silatrane analogs of indolylacetic acid (heteroauxin) and of synthetic phitohormones from phenoxyacetic acids. [Pg.348]

Amines which have two hydrogen atoms directly attached to a nitrogen atom, such as monoethanolamine (MEA) and 2-(2-aminoethoxy) ethanol (DGA), are called primary amines and are genially the most alkaline. Diethanolamine (DBA) and Diisopropanolamine (DIPA) have one hydrogen atom directly attached to the nitrogen atom and are called secondary amines. Triethanolamine (TEA) and Methyldiethanolamine (MDEA) represent completely substituted ammonia molecules with no hydrogen atoms attached to the nitrogen, and ate called tertiary amines. [Pg.42]

Dragendorff s reagent is a solution of iodobismuthate. It gives orange to red precipitates with tertiary amines, quaternary nitrogen, or sulfonium salts and alkaloids. Among aliphatic tertiary amines, triethanolamine, for example, does not react. [Pg.324]

The rate of stripping or the stripabiUty on cataly2ed urethane and epoxy resin finishes can be increased by adding formic acid, acetic acid, and phenol. Sodium hydroxide, potassium hydroxide, and trisodium phosphate [10101-89-0] may be added to the formula to increase the stripabiUty on enamel and latex paints. Other activators include oleic acid [112-80-17, trichloroacetic acid [76-85-9], ammonia, triethanolamine [102-71-6], and monoethyl amine. Methylene chloride-type removers are unique in their abiUty to accept cosolvents and activators that allow the solution to be neutral, alkaline, or acidic. This abihty gready expands the number of coatings that can be removed with methylene chloride removers. [Pg.551]

Gleaners. Properties, such as foaming and detergency (qv), make alkanolamines useflil in cleaning formulations. Monoetbanolamine is particularly effective in wax removal formulations because of its ability to penetrate films. Cleanets that involve skin contact use triethanolamine because of its mildness. Derivatives of the amines (49,50) as well as the free alkan olamines (51—53), may be formulated into cleaning products. [Pg.10]

Expert Panel of the Cosmetic Ingredient Review, Final Report on the Safety Assessment for Diisopropano/amine, Triisopropano/amine, Isopropano/amine, Mixed Isopropano/amines, Sept. 26, 1986 Final Report for the Safety Assessment for Triethanolamine, Diethanolamine, Monoethanolamine, May 19, 1983. [Pg.12]

Activated tertiary amines such as triethanolamine (TEA) and methyl diethanolamine (MDEA) have gained wide acceptance for CO2 removal. These materials require very low regeneration energy because of weak CO2 amine adduct formation, and do not form carbamates or other corrosive compounds (53). Hybrid CO2 removal systems, such as MDEA —sulfolane—water and DIPA—sulfolane—water, where DIPA is diisopropylamine, are aqueous alkaline solutions in a nonaqueous solvent, and are normally used in tandem with other systems for residual clean-up. Extensive data on the solubiUty of acid gases in amine solutions are available (55,56). [Pg.349]

The diisopropoxy-bis-(triethanolamine)-titanate, TYZORTE [36673-16-2] is an excellent cross-linker for aqueous solutions of hydroxyl-containing polymers. The reaction product of TYZORTPT with a mixture of trialkano1 amines and dialkanolarnines or monoalkano1 amines can be used to cure polyester-based powder coatings (109). Other ligands of this type iaclude triisopropano1 amine [122-20-3] ... [Pg.148]

Common examples of compounds that are amenable to carbon adsorption are aromatics (benzene, toluene) and chlorinated organics (trichloroethylene, trichloroethane [71-55-6, 75 -(9(9-j5y, tetrachloroethylene, polychlorinated biphenyls (PCBs), DDT /T(9-77-77, pentachlorophenol [87-86-5J. Compounds that are not adsorbed effectively by carbon include ethanol [64-17-5], diethylene glycol [111-46-6], and numerous amines (butylamine [109-73-9, 13952-84-6, 75-64-9], triethanolamine [102-71-6], cyclohexylamine [108-91-8], hexamethylenediamine [108-91-8] (1). Wastewater concentrations that are suitable for carbon adsorption are generally less than 5000 mg/L. [Pg.160]

With Ammonia and Amines. Ethylene oxide reacts with ammonia to form a mixture of mono-, di-, and triethanolamines. Nitrogen is a stronger nucleophile than oxygen (59). A small amount of water is essential for the reaction (60). [Pg.453]

Ethyl vinyl ether [109-92-2] M 72.1, b 35.5 , d 0.755. Contains polymerization inhibitors (usually amines, e.g. triethanolamine) which can be removed by fractional distn. Redistd from sodium. LACHRYMATORY. [Pg.242]

Formulated products tend to use a 10 to 20% neutralized erythorbate, buffered to pH of 5 to 6 with ammonia, morpholine, cyclohexy-lamine, diethanolamine (DEA), or triethanolamine (TEA) to reduce the acidity of erythorbic acid. Similarly, amines are used with sodium erythorbate to improve the reaction rate. [Pg.498]

Again both AE and LAS are effective in these types of liquids since they can be added to the formulation in a high-active, low-water form. LAB sulfonic acid can be neutralized in situ with a caustic or an amine base such as triethanolamine. [Pg.139]

One-phase titration methods have also been developed. These methods are not truly one-phase titrations but the term is used to indicate the absence of a second organic phase. One of these methods, applied to the analysis of sodium and triethanolamine lauryl sulfates and lauryl ether sulfates, use a quaternary amine as a titrant and cobalt(II) thiocyanate as indicator. Centrimide was found to avoid the use of chloroform which was not possible with other titrants examined, such as domiphen bromide and oxyphenonium bromide. The pink color of the indicator changes to violet as an excess of titrant forms a complex with the indicator [238]. [Pg.281]

The products of the chemical degradation of PETP with triethylene tetramine and triethaneolamine can be used as epoxy resin hardeners, it is demonstrated. Products of PETP aminolysis with triethylene tetramine and aminoglycolysis with triethanolamine, were characterised using NMR and rheometric measurements. Characteristics of the crosslinking process for the system epoxy resin/ PETP/amine degradation product, and epoxy resin/TETA for comparison were investigated by DSC. Three classes of liquid epoxy resins based on bisphenol A, bisphenol F and epoxy novolak resins were used in the experiments. 16 refs. [Pg.34]

Brononol (2-Bromo-2-nitropropane-1,3-diol) in combination with methyl and propyl paraben. The paper generated by the Danish group (ref. 5 Knoll BASF publication) shows that the mechanism of action of Bronopol is independent of formaldehyde formation. The inclusion of Tetrasodium EDTA at about 0.02% to remove ions in the water or extracts and carefully excluding any tertiary amines such as triethanolamine to counteract the fears of the marketers with reference to possible nitrosamine formation and release of formaldehyde. The pH used is usually at 6 and below. [Pg.158]

The most widely used amine is monoethanolamine (MEA), which is considered as a benchmark solvent because of its high cyclic capacity, significant absorption-stripping kinetic rates at low C02 concentration and high solubility in water. Some other amine-based solvents such as diethanolamine (DEA), triethanolamine (TEA), diglycolamine (DGA), N-methyldiethanol-amine (MDEA), piperazine (PZ), 2-amino-2-methyl-l-propanol (AMP) and N-(2-aminoeth-yl)piperazine (AEP) have also traditionally been utilised. [Pg.84]

The reaction is carried out in 0.2M triethanolamine, pH 8.2. DMS should be the limiting reagent in the reaction to avoid blocking all amines on both molecules with only one end of the... [Pg.892]

These are made by crosslinking unsaturated oils with sulphur (and an amine catalyst, usually triethanolamine) at 140-160 °C. These products will give dark coloured vulcanisates which have poor contact stain properties when in contact with painted surfaces. [Pg.141]

Silica fillers also react with the rubber causing an increase in viscosity and dry and unmanageable processing behaviour. Filler activators need to be added to silica-reinforced compounds to overcome these problems. The usual filler activators used are diethylene glycol, polyethylene glycol and amines such as triethanolamine. Some of these activators not only overcome the problems of processing and accelerator absorption, but depending on the cure system used, will also act as vulcanisation activators. [Pg.145]

Absorbents based on a variety of amines are by far the most common. Amines that have been used include monoethanolamine (MEA), diethanolamine (DEA), triethanolamine (TEA), diisopropanolamine (DIPA), methyl diethanolamine (MDEA), and digly-colamine (DGA). C02 is typically absorbed at 80-140°F temperature and up to 1000 psig pressure by chemically reacting with the basic amine functional group in the absorbent, for example, primary amine, MEA, reacts with C02 by the following reaction forming a carbamate salt ... [Pg.294]

Acetate, (C6H5)4AsC1, citrate, 2,3-dimercaptopropanol, EDTA, I-, Na5P3O10, SO)-, S20)-, tartrate, tiron, tetraphenylarsonium chloride, triethanolamine, thioglycolic acid Acetylacetone, citrate, CN-, EDTA, I-, NH3, N02, SCN-, S20)-, tartrate, triethanol amine Citrate, CN-, EDTA, I-, NH3, N02, SCN-, S20 -, tartrate, urea Reduction to Pu(IV) with sulfamic acid C20)-, citrate, EDTA, F-, tartrate Oxidation to perrhenate Citrate, tartrate, thiourea CN-, thiourea... [Pg.1445]


See other pages where Amines triethanolamine is mentioned: [Pg.185]    [Pg.92]    [Pg.420]    [Pg.16]    [Pg.641]    [Pg.1862]    [Pg.26]    [Pg.205]    [Pg.185]    [Pg.92]    [Pg.420]    [Pg.16]    [Pg.641]    [Pg.1862]    [Pg.26]    [Pg.205]    [Pg.164]    [Pg.1176]    [Pg.486]    [Pg.172]    [Pg.3]    [Pg.9]    [Pg.10]    [Pg.159]    [Pg.266]    [Pg.300]    [Pg.236]    [Pg.564]    [Pg.384]    [Pg.55]    [Pg.392]    [Pg.385]    [Pg.68]    [Pg.70]    [Pg.257]   
See also in sourсe #XX -- [ Pg.496 , Pg.562 ]




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