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Hydrogen temperature from

Figure 3.3 Distribution of double bonds at different hydrogenation temperatures. (From Cousins, E. R. Guice, W. A. Feuge, R. O. J. Am. Oil Chem. Soc. 1959, 36, 24. Reproduced with permission of AOCS Press.)... Figure 3.3 Distribution of double bonds at different hydrogenation temperatures. (From Cousins, E. R. Guice, W. A. Feuge, R. O. J. Am. Oil Chem. Soc. 1959, 36, 24. Reproduced with permission of AOCS Press.)...
A somewhat different type of high pressure reaction vessel is illustrated in Figs. VI, 4, 3-5. This is designed for hydrogenation reactions at working pressures from 1 to 300 atmospheres (4,500 lb. per square inch) and at temperatures from atmospheric up to 400°. Fig. VI, 4, 3... [Pg.869]

Dowtherm J is a mixture of isomers of an alkylated aromatic that contains only carbon and hydrogen. Dowtherm J can be used in Hquid-phase systems at temperatures as low as —73° C and in vapor-phase systems at temperatures from 185 to 315°C. Dowtherm Q is a mixture of diphenylethane and alkylated aromatics intended for Hquid-phase systems. It can be used at temperatures as low as —34°C. Dowtherm HT is a mixture of hydrogenated terphenyls intended for Hquid-phase systems. Dowtherm HT and Therminol 66 are essentially identical. [Pg.504]

The stabihty of pure hydrogen peroxide solutions increases with increasing concentration and is maximum between pH 3.5—4.5. The decomposition rate of ultrapure hydrogen peroxide increases 2.2—2.3-fold for each 10 °C rise in temperature from ambient to about 100 °C. This approximates an Arrhenius-type response with activation energy of about 58 kJ/mol (13.9 kcal/mol). However, decomposition increases as low as 1.6-fold for each 10 °C rise have been noted for impure, unstabilized solutions. [Pg.472]

The reaction of hydrogen and lithium readily gives lithium hydride [7580-67-8], LiH, which is stable at temperatures from the melting poiat up to 800°C. Lithium reacts with aitrogea, evea at ordiaary temperatures, to form the reddish browa nitride, Li3N. Lithium bums when heated in oxygen to... [Pg.223]

For feeds greater than 5 mol % hydrogen sulfide, but less than 40 mol %, the Recycle Selectox process can be used. In this variation of the Selectox process, a portion of the process gas leaving the condenser downstream of the Selectox reactor is recycled so as to limit the oudet gas temperature from the reactor to >205 C. [Pg.215]

Fig. 2. Behavior of electron-field emission at room temperature from Spindt-type arrays of 5000 tips per mm, beginning and ending with ultrahigh vacuum (UHV), eg, ultracontrol (UC) (a) water (b) hydrogen and (c) oxygen, where the dashed line indicates noise. To convert Pa to torr, divide by 133.3. Fig. 2. Behavior of electron-field emission at room temperature from Spindt-type arrays of 5000 tips per mm, beginning and ending with ultrahigh vacuum (UHV), eg, ultracontrol (UC) (a) water (b) hydrogen and (c) oxygen, where the dashed line indicates noise. To convert Pa to torr, divide by 133.3.
Arsenic pentasulfide (arsenic(V) sulfide), As S q, is stable in air up to 95°C, but at higher temperatures begins to dissociate into arsenous sulfide and sulfur. It is prepared by the fusion of arsenic with sulfur foUowed by extraction with ammonia and reprecipitation at low temperatures by addition of hydrochloric acid. Arsenic pentasulfide is precipitated at low temperatures from strongly acidic arsenate solutions by a rapid stream of hydrogen sulfide. It is hydrolyzed by boiling with water, yielding arsenous acid and sulfur. Salts derived from a number of thioarsenic acids are formed from arsenic pentasulfide and alkaH metal sulfides. [Pg.334]

Vulcanization. Generally this is carried out by the action of peroxides, which can cross-link the chains by abstracting hydrogen atoms from the methyl groups and allowing the resulting free radicals to couple into a cross-link. Some varieties of polysdoxanes contain some vinylmethyl siloxane units, which permit sulfur vulcanization at the double bonds. Some Hquid (short-chain) siHcones can form networks at room temperature by interaction between thek active end groups. [Pg.470]

Temperature The level of the temperature measurement (4 K, 20 K, 77 K, or higher) is the first issue to be considered. The second issue is the range needed (e.g., a few degrees around 90 K or 1 to 400 K). If the temperature level is that of air separation or liquefact-ing of natural gas (LNG), then the favorite choice is the platinum resistance thermometer (PRT). Platinum, as with all pure metals, has an electrical resistance that goes to zero as the absolute temperature decreases to zero. Accordingly, the lower useful limit of platinum is about 20 K, or liquid hydrogen temperatures. Below 20 K, semiconductor thermometers (germanium-, carbon-, or silicon-based) are preferred. Semiconductors have just the opposite resistance-temperature dependence of metals—their resistance increases as the temperature is lowered, as fewer valence electrons can be promoted into the conduction band at lower temperatures. Thus, semiconductors are usually chosen for temperatures from about 1 to 20 K. [Pg.1136]

Molecular dynamics simulations have also been used to interpret phase behavior of DNA as a function of temperature. From a series of simulations on a fully solvated DNA hex-amer duplex at temperatures ranging from 20 to 340 K, a glass transition was observed at 220-230 K in the dynamics of the DNA, as reflected in the RMS positional fluctuations of all the DNA atoms [88]. The effect was correlated with the number of hydrogen bonds between DNA and solvent, which had its maximum at the glass transition. Similar transitions have also been found in proteins. [Pg.448]

The peroxide decomposes at elevated temperatures to give free radicals, which then abstract a hydrogen atom from the methyl group. The radicals formed then combine to form a hydrocarbon linkage. Results obtained by reacting model systems with benzoyl peroxide and analysing the reaction products are consistent with this type of mechanism. ... [Pg.838]

For intermediate temperatures from 400-1000°C (Fig. 11), the volatilization of carbon atoms by energetic plasma ions becomes important. As seen in the upper curve of Fig. 11, helium does not have a chemical erosion component of its sputter yield. In currently operating machines the two major contributors to chemical erosion are the ions of hydrogen and oxygen. The typical chemical species which evolve from the surface, as measured by residual gas analysis [37] and optical emission [38], are hydrocarbons, carbon monoxide, and carbon dioxide. [Pg.414]

Decarburization results from hydrogen absorption from gas streams at elevated temperatures. In addition to hydrogen blistering, hydrogen can remove carbon from alloys. The particular mechanism depends to a large extent on the properties of other gases present. Removal of carbon causes the metal to lose strength and fail. [Pg.16]

Joly s method (or modifications) is the best procedure for preparing A " -3-ketones and can be extended to the elimination of hydrogen bromide from a-bromo ketones of all types. Rearrangement is sometimes observed but is not often serious. Selectivity can be improved in some instances by lowering the reaction temperature. The method has been found useful for the preparation of A" -3-ketones from 6-halo-A" -3-ketones ... [Pg.292]


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Hydrogen temperature

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