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Propylene glycol Specifications

Hydrolysis to Glycols. Ethylene chlorohydrin and propylene chlorohydrin may be hydrolyzed ia the presence of such bases as alkaU metal bicarbonates sodium hydroxide, and sodium carbonate (31—33). In water at 97°C, l-chloro-2-propanol forms acid, acetone, and propylene glycol [57-55-6] simultaneously the kinetics of production are first order ia each case, and the specific rate constants are nearly equal. The relative rates of solvolysis of... [Pg.73]

Figure 12.4 Propylene glycol in water, (a) Eutectic curve, (b) Density and specific heat capacity... Figure 12.4 Propylene glycol in water, (a) Eutectic curve, (b) Density and specific heat capacity...
What is the weight of 15 mL of propylene glycol having a specific gravity of 1.24 ... [Pg.34]

In many cases, the analytical tasks are simply to detect and quantify a specific known analyte. Examples include the detection and quantification of commonly used buffer components (e.g., Tris, acetate, citrate, MES, propylene glycol, etc.). These simple tasks can readily be accomplished by using a standard one-dimensional NMR method. In other situations, the analytical tasks may involve identifying unknown compounds. This type of task usually requires homonuclear and heteronuclear two-dimensional NMR experiments, such as COSY, TOCSY, NOESY, HSQC, HMBC, etc. The identification of unknown molecules may also require additional information from other analytical methods, such as mass spectrometry, UV-Vis spectroscopy, and IR spectroscopy.14... [Pg.309]

Fumaric and itaconic acids are also used as the diacid component. Most reaction formulations involve a mixture of a saturated diacid (iso- and terephthalic, adipic) with the unsaturated diacid or anhydride in appropriate proportions to control the density of crosslinking (which depends on the carbon-carbon double-bond content of the prepolymer) for specific applications [Parker and Peffer, 1977 Selley, 1988], Propylene glycol, 1,4-butanediol, neopentyl glycol, diethylene glycol, and bisphenol A are also used in place of ethylene glycol as the diol component. Aromatic reactants are used in the formulation to improve the hardness, rigidity, and heat resistance of the crosslinked product. Halogenated reactants are used to impart flame resistance. [Pg.119]

Spleen-derived B lymphocytes are then incubated with mouse myeloma cells in the presence of propylene glycol. This promotes fusion of the cells. The resultant immortalized antibody-producing hybridomas are subsequently selected from unfused cells by culture in a specific... [Pg.409]

Other Synthetic Fluids. Other synthetic fluids are used as heat-transfer fluids although most of them are not sold specifically for this purpose. Fluids that sometimes are used include diethylene glycol, triethylene glycol, propylene glycol, butyl carbitol, w -cymene, several silanes, several silicone fluids, some silicate fluids, other polyalkylene glycols, other oiganic ethers, and other molten salts. Fluidized solids also are used as heat-transfer media. [Pg.505]

Propylene glycol dinitrate is a colorless liquid of characteristic aromatic odor, more volatile and less viscous than trimethylene glycol dinitrate with which it is isomeric. Its specific gravity (20°/4°) is 1.368 at 20°. It boils at 92° at 10 mm., and does not freeze at —20°. Its solubilities, gelatinizing power, and explosive properties are substantially the same as those of its isomer. Indeed, Naoum 60 reports that it gave exactly the same expansion as trimethylene glycol dinitrate in the Trauzl lead block test, namely, 540 cc. [Pg.234]

Specifically, propylene oxide has reacted directly with maleic and phthalic anhydrides to produce unsaturated polyesters under these milder conditions (15, 16). This would certainly be a major first step toward simplifying the process and lowering the cost. Incidentally, use of propylene oxide in place of propylene glycol would also result in an additional saving of 1 cent per pound in total raw material cost as well (6). After polyesterification, the separate steps of cooling, dilution with styrene, catalysis, impregnation, gelation, and cure are a distinct operational and economic liability. [Pg.189]

Magnesium Stearate (or Octadecanolc acid magnesium salt). Mg(C18H3502)2 mw 591.27 soft white powder mp 88.5° specific gravity 1.028. Sol in chlf-propylene-glycol and hot benz. Prepn is by reacting a Mg salt (such as the acetate) with a soln of Na stearate. CA Registry No [557-04-0]... [Pg.440]


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