Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Temperature formation

In Section 8, the material on solubility constants has been doubled to 550 entries. Sections on proton transfer reactions, including some at various temperatures, formation constants of metal complexes with organic and inorganic ligands, buffer solutions of all types, reference electrodes, indicators, and electrode potentials are retained with some revisions. The material on conductances has been revised and expanded, particularly in the table on limiting equivalent ionic conductances. [Pg.1284]

Alcohol ethoxysulfates have been used in field tests as nitrogen (177) and carbon dioxide (178) foaming agents. Field use of alcohol ethoxysulfates is restricted to low temperature formations owing to its limited hydrolytic stabihty at low pH and elevated temperature (179). It has been reported that some foams can reduce residual oil saturation, not by oil displacement, but by emulsification and imbibition of the oil into the foam (180). [Pg.193]

When the host is a mixed oxide, the incorporation of the chromophore is best achieved during high temperature formation from single oxides ... [Pg.13]

The crude dibromohydrin distils without any decomposition at 10-15 pressure if the temperature of the oil bath is not raised over 190°. Above this temperature formation of acrolein derivatives begins, which, even if present in very small amounts, makes the dibromohydrin lachrymatory. [Pg.44]

Figure 4-5. Approximate hydrate temperature formation. Courtesy of Smith Industries, /nc.j... Figure 4-5. Approximate hydrate temperature formation. Courtesy of Smith Industries, /nc.j...
Special formulations have been developed for cementing operations in arctic regions or for deep water applications [206,208,256,720,739,1792]. In low-temperature formations, wherein the cement is subjected to freeze-thaw cycling, freezing-point depressants must be added. Salts may serve as such, but traditional organic freezing-point depressants, such as ethylene glycol, also may be added [1022-1024]. [Pg.133]

However, is supercomplex 27 the true intermediate As previously mentioned, Sugasawa reported that reaction did not proceed with N,N-dialkyl anilines. Do N,N-dialkylanilines form a similar supercomplex We examined the following three anilines, ArNH2, ArNHMe, and ArNMe2, as shown in Figure 1.3. Under Sugasawa conditions at room temperature, formation of the corresponding supercomplex, respectively (29,30, and 31) was confirmed, based on their NMR analyses (Complex 29 and 31 were derived from toluidine and complex 30 comes from aniline). [Pg.13]

The successful synthesis of diethyl phosphonomethyl triflate (193) is possible only at -15°C at higher temperatures formation of the ether (194) becomes important and exemplifies... [Pg.174]

A breaker an enzyme (at T<140°F), strong oxidizing agent, or an acid, is used to depolymerize polysaccharides and break crosslinks such that viscosity declines at a controlled rate so that the proppant may be deposited in the fracture. Too rapid proppant dropout would cause a premature "sand-out" which prevents future extension of the fracture. Peroxydisulfates are the most frequently used breakers. Less reactive organic peroxides may be preferred for high temperature formations (85). [Pg.18]

We have attempted the low temperature formation of Grignard reagents containing nitrile, ketone and ester functional groups. These reactions were largely unsuccessful, except in the case of 8-bromooctanenitrile. [Pg.240]

C. Graphite ordering increases with temperature. Formation of microcrystalline graphite and millimeter-size graphite crystals occurs above the eutectic point in the Fe/Fe3C system. [Pg.419]

When a gaseous flow of cyclopropylcarbinyl chloride is passed over NaY zeolite at room temperature, formation of cyclobutyl chloride and allylcarbinyl chloride was observed (scheme 4), as well as cyclopropylcarbinyl chloride (product and unreacted starting material). These data are consistent with formation of the C4H7+ cation with internal return of the chloride ion. [Pg.271]

Low temperature etching. Our data suggests that, under hydrothermal conditions the rate of pit formation is dramatically reduced, although perhaps not completely stopped, at C = Ccrjt. Etch pits on a natural, hydrothermally-etched quartz surface therefore indicate extended dissolution times, but not necessarily etching at C < Ccrit This is because the rate of etch pit formation even above Ccr t can be significant at elevated temperatures (as shown by crystal R9). However, at low temperatures, formation of etch pits when C > C would be less likely, and natural surfaces etched at low temperature should record the saturation state of the etching fluid. [Pg.642]

The first of the reaction steps in the amine-ozone interaction also consists of one-electron transfer from the amine to ozone, with the formation of the corresponding cation and anion-radicals. The ozone anion-radical has been revealed at low temperatures. Formation of the superoxide ion and the amine nitroxide are the understandable results of the reaction (Razumovskii and Zaikov 1984, reference therein). [Pg.58]

Fig. 19 shows that with increasing temperature, formation of 1, 5, and 7 benefit entropically and become substantially exoergic reactions. Formation of 3 and 4a exhibit little entropic benefit. As shown in Fig. 20, the reaction barriers similarly... [Pg.118]

Over the past two decades, important contributions to the chemistry of thiocarbonyl ylides were made by Huisgen et al. (27). By carrying out the reaction of thiobenzophenone with diazomethane at low temperature, formation of 2,5-dihydro-l,3,4-thiadiazole (15) with subsequent elimination of N2 was established as the route to the reactive thiobenzophenone (S)-methylide (16) (17,28). In the absence of intercepting reagents, 16 undergoes electrocyclization to give 17 or head-to-head dimerization to yield 1,4-dithiane 18 (Scheme 5.3). [Pg.318]


See other pages where Temperature formation is mentioned: [Pg.430]    [Pg.579]    [Pg.470]    [Pg.43]    [Pg.2]    [Pg.254]    [Pg.370]    [Pg.22]    [Pg.32]    [Pg.211]    [Pg.260]    [Pg.235]    [Pg.348]    [Pg.140]    [Pg.120]    [Pg.131]    [Pg.31]    [Pg.31]    [Pg.31]    [Pg.37]    [Pg.37]    [Pg.77]    [Pg.236]    [Pg.273]    [Pg.273]    [Pg.273]    [Pg.273]    [Pg.273]    [Pg.273]    [Pg.273]    [Pg.703]    [Pg.249]    [Pg.1]   
See also in sourсe #XX -- [ Pg.157 ]

See also in sourсe #XX -- [ Pg.489 , Pg.490 , Pg.491 ]

See also in sourсe #XX -- [ Pg.65 ]




SEARCH



Ankerite cement formation temperature

Arynes, mechanisms of formation and reactions at high temperatures

Char formation temperature effects

Enthalpy of formation high temperature

Filamentous carbon formation temperature effects

Film-formation temperature

Formation pressure, temperature, lithium

Formation rate temperature

Gibbs energy of formation high temperature

Glass formation temperature

Glass transition temperatures formation affected

High-temperature corrosion thermodynamics, formation

Hydrate Formation Temperature or Pressure

Micelle formation Krafft temperature

Minimum film formation temperature

Minimum film formation temperature MFFT)

Mutagen formation temperature

Onset temperature, polymer glass formation

Oxide layer formation, high-temperature corrosion

Oxide layer formation, high-temperature corrosion temperatures

Polymer glass formation temperature characteristics

Polymer glass formation temperature dependence

Polymer glass formation temperature effects

Supercooled liquids and glasses formation above glass transition temperature

Temperature alumina formation

Temperature and formation

Temperature of hydrates formation

Temperature on the formation

© 2024 chempedia.info