Ethyl fluid

ETHYL FLUID see MOTOR FUEL ANTI-KNOCK COMPOUND ... 

Th ese incidents compelled the U.S. Surgeon General to investigate the health effects of TEL. The industry itself moved rapidly to deal with the crisis by instituting a series of safety measures. Now, ethyl fluid was blended at distribution centers and not at seiMce stations (it had been done on the spot and increased the chances of lead poisoning to seiMce sta-... 

The material added to gasoline to increase octane was called ethyl fluid. A typical mixture contained the following 63% PbEt4, 26% Br— CH2—CH2—Br, 9% Cl—CH2—CH2—Cl, 2% dye (as a warning of its toxicity). About 1-6 ml of ethyl fluid was added per gallon of gasoline, depending on the octane number desired. Tetraethyllead apparently bums to form lead dioxide. 

Fig. 151. Continuous analysis of gasolines with ethyl fluid.

Ecole Nationale Superieure du Petrole et des Moteurs Formation Industrie end point (or FBP - final boiling point) electrostatic precipitation ethyl tertiary butyl ether European Union extra-urban driving cycle volume fraction distilled at 70-100-180-210°C Fachausschuss Mineralol-und-Brennstoff-Normung fluid catalytic cracking Food and Drug Administration front end octane number fluorescent indicator adsorption flame ionization detector... 

Difluoroethanol is prepared by the mercuric oxide cataly2ed hydrolysis of 2-bromo-l,l-difluoroethane with carboxyHc acid esters and alkaH metal hydroxides ia water (27). Its chemical reactions are similar to those of most alcohols. It can be oxidi2ed to difluoroacetic acid [381-73-7] (28) it forms alkoxides with alkaH and alkaline-earth metals (29) with alkoxides of other alcohols it forms mixed ethers such as 2,2-difluoroethyl methyl ether [461-57-4], bp 47°C, or 2,2-difluoroethyl ethyl ether [82907-09-3], bp 66°C (29). 2,2-Difluoroethyl difluoromethyl ether [32778-16-8], made from the alcohol and chlorodifluoromethane ia aqueous base, has been iavestigated as an inhalation anesthetic (30,31) as have several ethers made by addition of the alcohol to various fluoroalkenes (32,33). Methacrylate esters of the alcohol are useful as a sheathing material for polymers ia optical appHcations (34). The alcohol has also been reported to be useful as a working fluid ia heat pumps (35). The alcohol is available ia research quantities for ca 6/g (1992). 

Methyl- and dimethylnaphthalenes are contained in coke-oven tar and in certain petroleum fractions in significant amounts. A typical high temperature coke-oven coal tar, for example, contains ca 3 wt % of combined methyl- and dimethylnaphthalenes (6). In the United States, separation of individual isomers is seldom attempted instead a methylnaphtha1 ene-rich fraction is produced for commercial purposes. Such mixtures are used for solvents for pesticides, sulfur, and various aromatic compounds. They also can be used as low freezing, stable heat-transfer fluids. Mixtures that are rich in monomethyinaphthalene content have been used as dye carriers (qv) for color intensification in the dyeing of synthetic fibers, eg, polyester. They also are used as the feedstock to make naphthalene in dealkylation processes. PhthaUc anhydride also can be made from m ethyl n aph th al en e mixtures by an oxidation process that is similar to that used for naphthalene. 

Short-chain alkylated biphenyls are the principal biphenyl derivatives in commercial use. They are generally produced by Hquid-phase Friedel-Crafts alkylation of biphenyl with ethylene, propylene, or mixed butenes. A series of mixed ethylated biphenyl heat-transfer fluids (trademarked Therm S-600, 700, 800) is marketed by Nippon Steel. A mixed diethylbenzene—ethylbiphenyl heat-transfer fluid is also available from Dow (63). Monoisopropylbiphenyl [25640-78-2] largely as a mixture of meta- and para-isomers is produced by Koch Chemical Co. Monoisopropylbiphenyl (MIPB) was selected by Westinghouse (64,65) as a PCB replacement in capacitors and this is its primary appHcation today. For a time MIPB was also employed as a PCB replacement in pressure sensitive copy paper, but this outlet has since given way to other dye solvents. A similar product consisting of a mixture of j -butylbiphenyl isomers [38784-93-9] (66) is currently the favored dye solvent for pressure sensitive copy paper (67) manufactured in the United States. 

The formulation of calcium chelate materials is based upon the formation of a low-solubiUty chelate between calcium hydroxide and a sahcylate. Dycal utilizes the reaction product of a polyhydric compound and sahcyhc acid. Other sahcyhc acid esters can be similarly used. Vehicles used to carry the calcium hydroxide, extenders, and fillers may include mineral oil, A/-ethyl- -toluenesulfonamide [80-39-7] and polymeric fluids. The filler additions may include titanium dioxide [13463-67-7] zinc oxide, sihca [7631-86-9], calcium sulfate, and barium sulfate [7727-43-7]. Zinc oxide and barium sulfate are useflil as x-ray opacifying agents to ensure a density greater than that of normal tooth stmcture. Resins, rosin, limed rosins, and modified rosins may serve as modifiers of the physical characteristics in both the unset and set states. 

They show good to excellent resistance to highly aromatic solvents, polar solvents, water and salt solutions, aqueous acids, dilute alkaline solutions, oxidative environments, amines, and methyl alcohol. Care must be taken in choice of proper gum and compound. Hexafluoropropylene-containing polymers are not recommended for use in contact with ammonia, strong caustic (50% sodium hydroxide above 70°C), and certain polar solvents such as methyl ethyl ketone and low molecular weight esters. However, perfluoroelastomers can withstand these fluids. Propylene-containing fluorocarbon polymers can tolerate strong caustic. 

Elastomers formed using alkoxide salts of trifluoroethanol and higher fluoroalcohols have been found to have an interesting range of thermal and fluid resistance. These materials were developed under U.S. Army sponsorship, and initially commercialized by Firestone using the name PNF, later sold by Ethyl Corp. as EYPEL-F elastomer. ASTM has reserved the designation FZ for elastomers of this class which have the nominal stmcture given as (4). 

The estimated use pattern of ethyl ether during 1990 was as follows solvents and military production of smokeless powder, 35% chemical synthesis and solvent extraction, 35% diesel starting fluid, 30% (21). 

The concentration of a solute has a considerable effect on the viscosity of the fluid and so on the surface convective resistance to heat flow. There is little published data on these effects, so applications need to be checked from basic principles. Industrial alcohol (comprising ethyl alcohol with a statutory addition of methyl alcohol to render it poisonous) may be used as a secondary refrigerant, either at 100% concentration or mixed with water. The fluid has a low viscosity and good heat transfer, but is nowlittle used on account of its toxicity and the fire risk in high concentrations. Other nonfreeze heat transfer fluids are used in specialist trades. 

Tetraethyllead fluid in four gasolines supplied by the Ethyl Corporation was determined by the comparative method on weighed samples, aluminum serving as standard. These tetraethyllead fluids could have contained dibromo- or dichloroethane, or both, in addition to the lead compound. 

The values of x in column 4 were obtained by the Ethyl Corporation by a chemical method, for which the estimated precision is 0.02 ml of tetraethyllead fluid per gallon. Comparison of columns 4 and 5 shows agreement within these limits for all samples except B62M-3 the reason for the considerably greater discrepancy here is unknown. The precision of the x-ray work is better than was expected. (The precision is sufficiently great to warrant consideration of the difference in the x-ray absorption of the base stocks, samples AOT-1 and B62M-1.) Further-... 

A common approximation in many flow field computations at high fluid velocities is to consider that inertial forces dominate the flow and to neglect viscous forces (inviscid approximation). Since solvent viscosity is a variable in some of the experiments discussed here, the above approximation may be not be valid throughout and viscous forces are explicitly considered in the flow equations. Results of computations showed, nevertheless, that even with viscous solvents such as bis-(2-ethyl-hexyl)-phtalate with qi = 65 mPa s, viscous forces do not affect the flow field unless tbe fluid velocity drops below a few m s"1 at the orifice. This limit is generally more than one order of magnitude lower than the actual range used in the present investigations. 

For quantitative work, it is necessary to estimate the concentration of 5-amino-l-(P-D-ribofuranosyl)imidazole in aqueous solution. It seems that the only available method is the Bratton-Marshall assay, which was originally developed for the estimation of arylamines in biological fluids. The principle of the method is the spectrometric estimation of a salmon-pink colored dyestuff obtained by diazotation in situ, followed by coupling with /V-( 1 -naphthyl)ethyl-enediamine.65 The only remaining problem then is to know the molar extinction of this dye because pure samples of AIRs are not available. A value of 16800 at 520 nM was obtained for the dyes prepared from a model compound, 5-amino-l-cyclohexylimidazole-4-carboxylic acid (54), which is crystalline. A comparable molar extinction can be expected for the dye prepared from imidazole 55, if the carboxyl group does not exert too much influence on the chromophore. Actually, its influence is perceptible even with the naked eye, the dyestuff prepared from 53 having a somewhat different, wine-red color, with max>520 nM. The molar extinction for 55 is 17400 at 500 nM. When the decarboxylation of 54 was conducted under mild acidic conditions (pH 4.8, 50°C, 1 hour), estimation of 5-aminoimidazole 55 by the Bratton-Marshall method led to the conclusion that the reaction was almost quantitative.66 Similar conditions for the final decarboxylation were adopted in the preparation of samples of AIRs labeled with stable isotopes.58... 

P 5] Layers of 4,4 -bipyridyl (0.3 mol 1 in dichloromethane), ethyl bromoacetate (0.3 mol in dichloromethane) and a separation layer of dichloromethane were fitted into each other by means of a concentric separation mixer (three-fluid nozzle with three tubes having diameters of 1.5, 3 and 4 mm, slotted into each other) [78]. Thereby, two circular liquid layers of a thickness of 200 pm and a center stream of 1.5 mm diameter were generated. The reaction temperature was 22 °C. The reaction solution was inserted as droplets or a continuous stream either directly or via... 

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