Triethanolamine effect

Chemical Properties. Trimethylpentanediol, with a primary and a secondary hydroxyl group, enters into reactions characteristic of other glycols. It reacts readily with various carboxyUc acids and diacids to form esters, diesters, and polyesters (40). Some organometaUic catalysts have proven satisfactory for these reactions, the most versatile being dibutyltin oxide. Several weak bases such as triethanolamine, potassium acetate, lithium acetate, and borax are effective as stabilizers for the glycol during synthesis (41). 

The most widely used alkyl sulfate in shampoo preparation is lauryl sulfate. The alkyl component of this sulfate ranges from C-10 to C-18 with a predominance of the C-12 (lauryl) component. By distillation of the fatty alcohol, certain cuts can be obtained which offer the best effects in foaming, cleansing, and rinsing properties for the alkyl sulfate preparation. The range which appears to be most desirable is between C-12 and C-16. Lauryl sulfate detergents are available in various salt forms with the sodium, ammonium, and triethanolamine types being used most frequently in shampoos. 

In concrete, triethanolamine accelerates set time and increases early set strength (41—43). These ate often formulated as admixtures (44), for later addition to the concrete mixtures. Compared to calcium chloride, another common set accelerator, triethanolamine is less corrosive to steel-reinforcing materials, and gives a concrete that is more resistant to creep under stress (45). Triethanolamine can also neutralize any acid in the concrete and forms a salt with chlorides. Improvement of mechanical properties, whiteness, and more even distribution of iron impurities in the mixture of portland cements, can be effected by addition of 2% triethanolamine (46). Triethanolamine bottoms and alkanolamine soaps can also be used in these type appUcations. Waterproofing or sealing concrete can be accompUshed by using formulations containing triethanolamine (47,48). 

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. 

Pigment Dispersion. The alkan olamines and thek derivatives are useful in dispersing titanium dioxide and other pigments (209). Monoisopropanolamine and triethanolamine are particularly effective in aiding titanium dioxide dispersion in the production of Ti02 and in water-based paints (210). The alkan olamines are also an aid in the grinding of titanium dioxide (211). 

In Cosmetics. Amino acids and their derivatives occur in skin protein, and they exhibit a controlling or buffering effect of pH variation in skin and a bactericidal effect (216). Serine is one component of skin care cream or lotion. Ai-Acylglutamic acid triethanolamine monosalt is used for shampoo. Glucose glutamate is a moisturizing compound for hair and skin (234). 

Nonblack fillers such as the precipitated siHcas can reduce both rate and state of cure. The mechanism appears to be one of a competitive reaction between mbber and filler for the zinc oxide activator. Use of materials such as diethylene glycol or triethanolamine prevents this competition thereby maintaining the desired cure characteristics. Neutral fillers such as calcium carbonate (whiting) and clays have Httie or no effect on the cure properties. 

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. 

The hydrolysis of phosphites is retarded by the addition of a small amount of a base such as triethanolamine. A more effective approach is the use of hindered phenols for esterification. Relatively good resistance to hydrolysis is shown by two esters derived from hindered phenols tris(2,4-di-/ / butylphenyl)phosphite [31570-04-4] (25) and tetrakis(2,4-di-/ /f-butylphenyl)4,4 -biphenylenediphosphonite [38613-77-3] (26). The hindered fluorophosphite [118337-09-0] (27) has excellent resistance to hydrolysis. 

Deprotonation of enols of P-diketones, not considered unusual at moderate pH because of their acidity, is faciUtated at lower pH by chelate formation. Chelation can lead to the dissociation of a proton from as weak an acid as an aUphatic amino alcohol in aqueous alkaU. Coordination of the O atom of triethanolamine to Fe(III) is an example of this effect and results in the sequestration of iron in 1 to 18% sodium hydroxide solution (Fig. 7). Even more striking is the loss of a proton from the amino group of a gold chelate of ethylenediamine in aqueous solution (17). 

For many years such media have been based on strong salt solutions, e.g. calcium chloride brines. Sodium dichromate has been used (seep. 17 26), but recently other inhibitors have been claimed to be effective. One patent quotes N-alkyl-substituted alkanolamines, e.g. 2-ethyl ethanolamine -I- BTA at pH A mixture of hydrazine hydrochloride -i- BTA has been claimed as well as a mixture of gelatin -h triethanolamine -h potassium dihydrogen phosphate . Other examples are to be found in the patent literature and the above are quoted to illustrate the diversity of chemicals that may be used. 

Cu, Ni, Co, Cr, Fe, or Al, even in traces, must be absent when conducting a direct titration of the other metals listed above if the metal ion to be titrated does not react with the cyanide ion or with triethanolamine, these substances can be used as masking reagents. It has been stated that the addition of 0.5-1 mL of 0.001 M o-phenanthroline prior to the EDTA titration eliminates the blocking effect of these metals with solochrome black and also with xylenol orange (see below). 

Most of the LAB sulfonic acid that is produced is neutralized to the Na+ salt. However, sulfonic acid can be neutralized with other bases to make different salts such as NH4+, TEA+ (triethanolamine), Mg2+, among others. In the latter 1970s, a major U.S. laundry liquid contained about 20-25% Mg(LAS)2 as the major active ingredient, along with a smaller amount of TEA+ salt of LAS [17]. This product was reported to be a very effective detergent on oily or greasy soils. 

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. 

A mixture of monolauryl phosphate sodium salt and triethylamine in H20 was treated with glycidol at 80°C for 8 h to give 98% lauryl 2,3-dihydro-xypropyl phosphate sodium salt [304]. Dyeing aids for polyester fibers exist of triethanolamine salts of ethoxylated phenol-styrene adduct phosphate esters [294], Fatty ethanolamide phosphate surfactant are obtained from the reaction of fatty alcohols and fatty ethanolamides with phosphorus pentoxide and neutralization of the product [295]. A double bond in the alkyl group of phosphoric acid esters alter the properties of the molecule. Diethylethanolamine salt of oleyl phosphate is effectively used as a dispersant for antimony oxide in a mixture of xylene-type solvent and water. The composition is useful as an additive for preventing functional deterioration of fluid catalytic cracking catalysts for heavy petroleum fractions. When it was allowed to stand at room temperature for 1 month it shows almost no precipitation [241]. 

The GMT in human serum reacts most rapidly with Y-glutamyl-p-nitroanilide at pH 8.2. The same activity is found in 2-amino-2-methylpropane-l 3 diol, diethanolamine, triethanolamine and tris buffers. Magnesium ions have no effect on the activity but favor the solubilization of the substrate. Bondar and Moss (54) found that free glutamate, due to elevated serum glutamate concentrations or glutamate released by substrate breakdown, increases the apparent GMT activity. They concluded that the assay should be performed in the presence of 1.0 vM/1 glutamate in order to reduce the possibility of falsely elevated results. This was not observed by others. Rowe and co-workers have indicated that certain batches of p-nitroanilide substrate contain impurities which may reduce GMT activity and increase the values ( ). Huesby and Stromme (56) confirmed the presence of such impurities and recommended pyridine extraction for substrate purification. 

ADCA is activated by zinc oxide, zinc stearate (strongly) and urea (slowly). Barium stearate, calcium stearate and triethanolamine, when added at 10 phr, moderately activate gas evolution from ADCA. They do not have very much effect on decomposition rate when the cure temperature is at 170 °C, but a marked effect above 180 °C. The rate of decomposition of ADCA is significantly influenced by the particle size of the additive. Effective dispersion and heat transfer through the particle can be a means of controlling the cell quality and the manufacturing method for the product. The correct particle size is selected to achieve the optimum balance between cure and cell development. 

The massive contamination of NDE1A in alkaline synthetic fluids (3%) found by Fan et al Q) cannot be explained by known nitrosation kinetics of di- or triethanolamine. Instead, more powerful nitrosation routes, possibly involving nitrogen oxide (N0X) derivatives (e.g., N02> N O t) may be responsible for the amounts of NDE1A in these products (34). In fact, a nitrite-free commercial concentrate was shown to accumulate NDE1A up to about 10 0 days at which time the levels dropped dramatically (19). Inhibition of N0X contaminants may be an effective route to the inhibition of nitrosamine formation in metalworking fluids. 

As a consequence of the detection of catalytic pathways for formation of PCDD/F, special inhibition methods have been developed for PCDD/F. By this approach the catalytic reactions are blocked by adding special inhibitors as poisoning compounds for copper and other metal species in the fly ash. Special aliphatic amines (triethylamine) and alkanolamines (triethanolamine) have been found to be very efficient as inhibitors for PCDD/F, and have been used in pilot plants. The effect can be seen in Figure 8.6. The inhibitors have been introduced into the incinerator by spraying them into the postcombustion zone of the incinerator at about... 

FIGURE 5 The effect of the BGE concentration on the enantiomeric separation of ropivacaine. (A) BGE SOmM phosphoric acid, 44mM triethanolamine, lOmM DM-/7-CD. (B) BGE lOOmM phosphoric acid, 88 mM triethanolamine, lOmM DM-/I-CD (with permission from reference 56). 

The membrane surface may become passivated by some solution components that are strongly adsorbed. This effect is often encountered in measurements on biological fluids containing proteins. These adsorption effects can sometimes be prevented by selecting a suitable compoation of the sample and standard solutions for example by adding trypsin and triethanolamine to dissolve proteins [108]. Passive electrodes can sometimes be reactivated by soaking in suitable solutions (for example pepsin in 0.1M HCl [68]) and in more serious cases the membrane must be replaced or a solid membrane be repolished. 

Until now syntheses along path d) of Figure 3 are known only for small bicyclic systems, for instance N(CH2CH20)3B from triethanolamine and B(OH)3 (87), N(CH2CH2CH2)3B from triallylamine and BH3 (88). However, macrobicyclic structures may be obtained in this way from a tripod type structure by making use of the template effect of a complexed transition metal cation, which remains included in the product (89-91). 

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