Plasticizers triethanolamine

Electrodeposition has been attempted also on flexible substrates within the scope of fabricating flexible solar cells. Huang et al. [177] investigated the electrodeposition of CIS on Au-coated plastic substrate from aqueous acidic (pH 1.65) solutions of millimolar CuCh, InCb, Se02, containing triethanolamine and sodium citrate. Stoichiometric, semiconductive CIS films (Eg = 1.18 eV) were obtained after annealing at 150 °C in nitrogen. 

Organic compounds derived from ethanol and amino groups (—NH2). See Triethanolamine. Ethenoid Plastics... 

P.R. deWilde, BritP 882555(1961) CA 56, 11876(1962) [A plastic explosive prepd by intimately mixing AN >60, a nitrate of an alkylamine (such as that of mono-, di-, or triethanolamine = 8, H2O up to 15% and dispersing thruout the dough-like mixt, so obtd,... 

The Dylux 503 formulation contained a HABI, the leucodye TLA-454, a mixture of quinones, triethanolamine triacetate, several plasticizers, an organic acid, cellulose acetate butyrate binders, as well as antiblocking agents (fluorinated derivatives) as well as a silica derivative to provide tooth to the coating. The selection was made to provide maximum performance at minimum mill cost. The paper substrate required had high holdout, so as to permit two-sided coatings as well as to minimize the wicking of chemistry into the base. 

In topical formulations, stearic acid is used as an emulsifying and solubilizing agent. When partially neutralized with alkalis or triethanolamine, stearic acid is used in the preparation of creams. The partially neutralized stearic acid forms a creamy base when mixed with 5-15 times its own weight of aqueous liquid the appearance and plasticity of the cream being determined by the proportion of alkali used. 

Triethanolamine is used as an intermediate in the manufacturing of surfactants, textile specialties, waxes, polishes, herbicides, petroleum demulsifiers, toilet goods, cement additives, and cutting oils. Triethanolamine is also claimed to be used for the production of lubricants for the rubber gloves and textile industries. Other general uses are as buffers, solvents, and polymer plasticizers, and as a humectant. 

The other approach is to embed the hygroscopic perchlorates in a plastic material, which thus becomes fuel, binder, and protective coating and also opens the way for new production techniques. This scheme has been tried as shown in a U. S. patent for lithium perchlorate embedded in nylon for the purpose of formulating high-energy propellants, and it is applicable to colored flame production. A similar idea is incorporated in another U. S. patent that deals with colored flame matches or more exactly match splints made from cellulose acetate in which the perchlorates of copper or strontium perchlorate, dissolved in triethanolamine, are dispersed. Again, the color effect is most pleasing, but the technique seems to have remained confined to laboratory samples. 

Besides sensitization to (meth)acrylates, relevant sources of occupational allergic contact dermatitis are initiators, accelerators, catalysts, inhibitors and pigments of dental plastics. In particular, hydroqui-none, hydroquinone monomethylether, campherqui-none, N,N-dimethyl-p-toluidine, triethanolamine, (4-methoxyphenol) benzoylperoxide, chinacridone B, catalysts of Impregum and Scutan and various (di)amines, barbiturates and benzoates have been identified as occupationally relevant sensitizers (Jolanki et al. 1987 Niklasson and Bjorkner 1989 Tosti et al. 1993 Richter 1996). 

Kushi and Handa (68) described in 1985 a TLC/MS method for the analysis of lipids. Secondary ion mass spectrometry with a liquid matrix of triethanolamine was used for the extraction and ionization of sample spots first located with iodine or Coomassie brilliant blue staining. A piece of TLC plate of size 5 x 20 mm could be attached to the direct insertion probe, and scanning in one-dimension was accomplished by manually inserting the probe into the source of the mass spectrometer. Spectra could be obtained from one microgram of a lipid separated on a silica TLC plate with aluminum- or plastic-backed TLC plates. Although not specifically noted in this paper, since a plastic-backed plate is an electrical insulator, some provision for connecting the surface to the plate platform itself must be made to hold the surface at the source potential. 

Additives used in final products Fillers aluminosilicate, calcium carbonate, clay, mica, talc Plasticizers acetyl triethyl citrate, benzyl butyl phthalate, dibutyl phthalate, castor oil, dipropylene glycol dIbenzoate, epoxidized soybean oil, ethylene and propylene glycols, glycerin, triethanolamine, triacetin, tributyl citrate, trIethyl citrate Antistatic quaternary ammonium salt Release zinc stearate ... 

In [75,76], a method of decomposition of polyurethane rigid foams is described, using EG, DEG, and polyoxypropylenated pentaerythritol (with a hydroxyl number of 170 mg KOH/g) mixed with ethanolamines (mono-, di- and triethanolamine). Various salts of metals, such as tin, iron, sodium, potassium, zinc, calcium, copper, and cobalt were used as catalysts. The process products can be used as raw materials for the production of polyurethane plastics. 

April 5, 1972 (Cl. 430/343 430/524 430/531 430/538). Appl. 99,512, December 18, 1970, 15 pp. Improved photosensitive compositions comprising A. an acid salt of a leuco aminotriarylmethane such as tris(4-N,N-diethylamino-o-tolyl)methane B. a hexaarylbiimidazole such as a 2,2 -bis(o-chloro-phenyl)-4,4 5,5 -tetraphenylbiimidazole and C. a redox couple containing (1) as an oxidant a polynuclear quinone absorbing principally in the 400-550 nm region such as 1,6-pyrenequinone, and (2) as a reductant an acyl ester of triethanolamine such as triethanolamine triacetate optionally mixed with a lower alkyl ester of a nitrilotrialkanoic acid such as 3,3, 3"-nitrilotripropionic acid, trimethyl ester are effective color forming compositions useful in a variety of applications. The need for an effective plasticizer system was solved by the addition of sulfonamides and ethoxylated phenol derivatives. 

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