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Glycol ethers conductivity

Cancer. No studies were located regarding carcinogenic effects in humans or animals after exposure to 2-butoxyethanol, 2-butoxyethanol acetate, or 2-butoxyacetic acid by any route. However, structure-activity studies with 2-butoxyethanol and eight other glycol ethers were conducted with a cellular leukemia transplant model in male Fischer 344 rats to determine the chemotherapeutic potential of these glycol ethers (Dieter et al. 1990). 2-Butoxyethanol was administered ad libitum in the drinking water to... [Pg.275]

Since 27 possible combinations of resin and solvent were possible, each solvent resin system could not be examined over a wide range of concentrations. Accordingly, the investigation was conducted in two parts. In the first part all possible combinations of resin and solvent were evaluated at 70% non-volatile concentration. In the second part the solvents which appeared the most interesting were examined at other concentrations. The glycol ethers generally proved to be the most versatile for electrodeposition. As the studies progressed, however, certain other areas of interest developed which may be worthy of future study. [Pg.150]

In general, all hydrocarbons and ethers (but not glycol ethers) have conductivities of 1 pico-siemen/cm or less and are liable to generate static electricity. The higher molecular weight esters are at or near the limit. The unit used in the tables is siemen/cm. [Pg.8]

Electrophoretic coatings are similar to those used and described in section 8.2 on automotive OEM coatings. Metallic (conductive) substrates are essential if this technique is to be used successfully. Water is obviously the main solvent to achieve the degree of conductivity needed, but significant quantities of solvents such as the glycol ethers are needed to solubilise the resins used and to produce the quality of film finish required. [Pg.170]

In the electrodeposition coating process electrically chaiged resin particles are deposited onto a conductive metal surface from a water dispersion. Glycol ethers serve as a resin solvent in the coating preparation step and as a coalescent solvent during film formation. Glycol ethers used in the electrodeposition process include EB, DB, PM, and PPh. [Pg.208]

Multi-armed polymers with a cyclotriphosphazene core XI and XII have been synthesized from the reaction of polyethylene glycol monomethyl ethers with acid chlorides of hexakis(3,5-dicarboxyphenoxy) and hexakis(4-carboxyphe-noxy) cyclotriphosphazenes. Their complexes with LiC104 were investigated, and their maximum conductivities are reported in Table 17 [621]. [Pg.210]

Polyphosphazenes sulfonates XIX with the anion covalently attached to the polymer are a new class of cation conductors that have been synthesized by Shriver [625]. They were obtained by reaction of Na0C2H4S03Na with an excess of polydichlorophosphazene in the presence of 15-crown-5, followed by the reaction of the partially substituted product with the sodium salt of poly(ethylene glycol methyl ether). The conductivity at 80 °C of the polymer with x=1.8, m=7.22 is 1.7x10 S cm This low conductivity can be attributed to an extensive ion pair formation between the sodium and sulfonate ions. [Pg.212]

Corexit 9527 is a water-and ethylene glycol monobutyl ether-dissolved dispersant. The nature of the surface-active agent has not been disclosed. Laboratory tests were conducted using 0.5-mm thick, fresh Alberta Sweet-Mixed Blend crude oil treated with Corexit 9527 dispersant applied from an overhead spray boom [165]. The effects on dispersion efficiency of mixing jet pressure, mixing jet flow rate, jet standoff distance, and vessel speed were evaluated. The system operates with a nozzle pressure of 7000 kPa, a flow rate of 55 liter/min per nozzle, and nozzles positioned approximately 0.6 m from the water surface. In laboratory tests, such a system was capable of dispersing 80% to 100% of the surface slick. [Pg.296]

Glycolysis is also conducted to create polyols for unsaturated polyester usage. The PET can be dissolved in DEG to create polyols with ether linkages [30], The reaction can be carried out with propylene glycol [31] or by reacting with an unsaturated dibasic acid [32] and needed additives and catalysts [33],... [Pg.572]

When labeled potassium cyanide reacted with the complex in an aqueous methanol solution, the bromide was rapidly replaced and the labeled cyanide ion entered slowly into the coordination complex. When the reaction was conducted at higher temperatures in ethylene glycol dimethyl ether as the solvent, the label was distributed among the benzyl isonitrile, benzyl formamide, and the polymer resulting from benzyl isonitrile and the iron isonitrile complexes. [Pg.110]

Fatty acid esters would be predicted to have little irritation or toxic effects. Ex vivo permeability studies conducted in porcine buccal mucosa showed significant permeation enhancement of an enkephalin from liquid crystalline phases of glycerine monooleate [32]. These were reported to enhance peptide absorption by a cotransport mechanism. Diethylene glycol monoethyl ether was reported to enhance the permeation of essential oil components of Salvia desoleana through porcine buccal mucosa from a topical microemulsion gel formulation [33]. Some sucrose fatty acid esters, namely, sucrose laurate, sucrose oleate, sucrose palmitate, and sucrose stearate, were investigated on the permeation of lidocaine hydrochloride [34], with 1.5% w/v sucrose laurate showing a 22-fold increase in the enhancement ratio. [Pg.207]


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Glycols/glycol ethers

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