Big Chemical Encyclopedia

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

Articles Figures Tables About

Terminal cracking

Table ID. Terminal Cracking Index and Benzene Selectivity Parameter at 733 K... Table ID. Terminal Cracking Index and Benzene Selectivity Parameter at 733 K...
Impregnation of Pt/Mg(Al)0 with aqueous KOH resulted in a greater selectivity toward benzene production and a significant increase in the terminal cracking index. The large effect of KOH is attributed to the neutralization of surface acid sites, alkali... [Pg.335]

Although little research has been reported on the effects of fillers on crack propagation rates, DiBenedetto (1973) and Peretz and DiBenedetto (1972) have investigated the behavior of rapidly growing cracks in epoxy resins filled with glass beads and in a rubber-modified epoxy resin. In both the unfilled and the bead-filled resins, the terminal crack velocity... [Pg.404]

Alternatively, thermolysis yields the terminal alkene RCH=CH2. Note that, if propene or higher alkenes are u.sed instead of ethene, then only single insertion into Al-C occurs. This has been commercially exploited in the catalytic dimerization of propene to 2-methylpentene-1, which can then be cracked to isoprene for the production of synthetic rubber (cu-1,4-polyisoprene) ... [Pg.260]

Many engineering thermoplastics (e.g., polysulfone, polycarbonate, etc.) have limited utility in applications that require exposure to chemical environments. Environmental stress cracking [13] occurs when a stressed polymer is exposed to solvents. Poly(aryl ether phenylquin-oxalines) [27] and poly(aryl ether benzoxazoles) [60] show poor resistance to environmental stress cracking in the presence of acetone, chloroform, etc. This is expected because these structures are amorphous, and there is no crystallinity or liquid crystalline type structure to give solvent resistance. Thus, these materials may have limited utility in processes or applications that require multiple solvent coatings or exposures, whereas acetylene terminated polyaryl ethers [13] exhibit excellent processability, high adhesive properties, and good resistance to hydraulic fluid. [Pg.56]

The secondary free radical can crack on either side of the carbon carrying the unpaired electron according to the beta scission rule, and a terminal olefin is produced. [Pg.56]

The newly formed free radical may terminate by abstraction of a hydrogen atom, or it may continue cracking to give ethylene and a free radical. Aromatic compounds with side chains are usually dealkylated. The produced free radicals further crack to yield more olefins. [Pg.92]

Riser termination. Good riser termination devices, such as closed cyclones, minimize the vapor and catalyst holdup time in the reactor vessel. This reduces unnecessary thermal cracking and nonselective catalytic re-cracking of the reactor product. The benefits are a reduction in dry gas and a subsequent improvement in conversion, gasoline octane, and flexibility for processing marginal feeds. [Pg.203]

At the request of an international petroleum company, a major manufacturer and supplier of down-hole equipment performed tests of the various elastomers commonly used in the construction of packers and other oil field tools. Seven of the nine most commonly used thermoplastic materials were found to be completely inert to TKPP solutions. The test included continual immersion in saturated TKPP for 21 days at 280°F. Only two elastomers, Vi-ton and Fluorel, showed any adverse reaction. O-rings made from these two elastomers showed minor cracking at the termination of the test. A listing of the elastomers that tested inert to TKPP solutions include nitrile, saturated nitrile (HNBR), Aflas, Kalrez, PEEK, Glass-filled Teflon, and Ryton. Several of these elastomers are attacked or degraded by conventional clear completion fluids containing calcium and zinc halides. The inertness of commonly employed elastomers to TKPP is an important advantage for TKPP fluids in normal operations. [Pg.632]

The condensed cycloparaffin rings crack yielding n-butyl groups, containing, in part, the 13C label in a terminal CHg position (signal at 14.0). [Pg.376]

The hydrocarbon catalytic cracking is also a chain reaction. It involves adsorbed carbonium and carbenium ions as active intermediates. Three elementary steps can describe the mechanism initiation, propagation and termination [6]. The catalytic cracking under supercritical conditions is relatively unknown. Nevertheless, Dardas et al. [7] studied the n-heptane cracking with a commercial acid catalyst. They observed a diminution of the catalyst deactivation (by coking) compared to the one obtained under sub-critical conditions. This result is explained by the extraction of the coke precursors by the supercritical hydrocarbon. [Pg.350]

The answer is b. (Kn.lzu.ng, p 5.38.) Crack is the free-base (nonsalt) form of the alkaloid cocaine. It is called crack because, when heated, it makes a crackling sound. Heating crack enables a person to smoke it the drug is readily absorbed through the lungs and produces an intense euphoric effect in seconds Use has led to seizures and cardiac arrhythmias. Some of cocaine s effects (sympathomimetic) are due to blockade of norepinephrine reuptake into presynaptic terminals it does not block receptors. Flashbacks can occur with use of LSD and mescaline but have not been associated with the use of cocaine. [Pg.160]


See other pages where Terminal cracking is mentioned: [Pg.327]    [Pg.328]    [Pg.333]    [Pg.334]    [Pg.335]    [Pg.196]    [Pg.196]    [Pg.218]    [Pg.113]    [Pg.405]    [Pg.1230]    [Pg.327]    [Pg.328]    [Pg.333]    [Pg.334]    [Pg.335]    [Pg.196]    [Pg.196]    [Pg.218]    [Pg.113]    [Pg.405]    [Pg.1230]    [Pg.202]    [Pg.365]    [Pg.467]    [Pg.203]    [Pg.66]    [Pg.508]    [Pg.505]    [Pg.359]    [Pg.345]    [Pg.30]    [Pg.1365]    [Pg.15]    [Pg.10]    [Pg.93]    [Pg.305]    [Pg.102]    [Pg.104]    [Pg.105]    [Pg.106]    [Pg.142]    [Pg.151]    [Pg.51]    [Pg.1174]   
See also in sourсe #XX -- [ Pg.218 ]




SEARCH



© 2024 chempedia.info