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Methylpentanes, catalytic cracking

Fig. 5.1. Chromatograms of products of catalytic cracking (A) without reactor and (B) with reactor. Sorbent, 11% quinoline on refractory brick temperature, 25 C column length, 10.5 m. Peaks 1 = propane 2 = propylene 3 = isobutane 4 = n-butane 5 = isobutene 6 = butene-1 7 = rmns-butene-2 8 = cis-butene-2 9 = isopentane 10 = 3-methylbutene-l 11 = n-pentane 12 = pentene-1 13 = 2,2-dimethylbutene 14 = 2-methylbutene-l 15 = tnms-pentene-2 16 = cfsi)entene-2 17 = 2-methyl-butene-2 18 = 2,3-dimethylbutane 19 = 2-methylpentane 20 = 3-methylpentane 21 = 3-methylpen-tene-1 22 = 4-methylpentene-l 23 = c -4-methylpentene-2 24 = cyclopentane 25 = 2,3-dimethyl-butene-1 26 = fmns-4-methylpentene-2 27 = w-hexane 28 = cyclopentene 29 = 2-methylpentene-l 30 = hexene-1 31 = 2,4-dimethylpentane 32 = cis-hexene-3 33 = tnms-hexene-3 34 = 2-ethylbu-tene-1 35 = trans-hexene-2 36 = methylcyclopentane 37 = cis-methylpentene-2 38 = 2-methylpen-tene-2 39 = pisns-3-methylpentene-2 40 = methylcyclopentene-4 41 = 4-methylcyclopentene 42 = cw-3-methylpentene-2 43 = 2,3-dimethylpentane 44 = 2-methylheptane 45 = 2,3-dimethylbutene-2 46 = methylheptane 47 = cyclohexane 48 = C, olefin. Reprinted with permission from ref. 1. Fig. 5.1. Chromatograms of products of catalytic cracking (A) without reactor and (B) with reactor. Sorbent, 11% quinoline on refractory brick temperature, 25 C column length, 10.5 m. Peaks 1 = propane 2 = propylene 3 = isobutane 4 = n-butane 5 = isobutene 6 = butene-1 7 = rmns-butene-2 8 = cis-butene-2 9 = isopentane 10 = 3-methylbutene-l 11 = n-pentane 12 = pentene-1 13 = 2,2-dimethylbutene 14 = 2-methylbutene-l 15 = tnms-pentene-2 16 = cfsi)entene-2 17 = 2-methyl-butene-2 18 = 2,3-dimethylbutane 19 = 2-methylpentane 20 = 3-methylpentane 21 = 3-methylpen-tene-1 22 = 4-methylpentene-l 23 = c -4-methylpentene-2 24 = cyclopentane 25 = 2,3-dimethyl-butene-1 26 = fmns-4-methylpentene-2 27 = w-hexane 28 = cyclopentene 29 = 2-methylpentene-l 30 = hexene-1 31 = 2,4-dimethylpentane 32 = cis-hexene-3 33 = tnms-hexene-3 34 = 2-ethylbu-tene-1 35 = trans-hexene-2 36 = methylcyclopentane 37 = cis-methylpentene-2 38 = 2-methylpen-tene-2 39 = pisns-3-methylpentene-2 40 = methylcyclopentene-4 41 = 4-methylcyclopentene 42 = cw-3-methylpentene-2 43 = 2,3-dimethylpentane 44 = 2-methylheptane 45 = 2,3-dimethylbutene-2 46 = methylheptane 47 = cyclohexane 48 = C, olefin. Reprinted with permission from ref. 1.
The cracking pattern on Pt-Ce is similar to the one observed on Platinum catalysts on Pt-Co catalysts, the demethylation reaction is more important than on Pt catalyst. When Ni is added, repetitive cracking reactions occur the ratio of isobutane over n-butane is lower than 1 on these latter catalysts which means that multiple processes occur on the catalytic surface because n-butane cannot be obtained from 2-methylpentane with only one carbon-carbon bond breaking. [Pg.248]

The catalytic characterization of zeolites is generally carried out with the aid of test reactions [8]. For example, the constraint index Cl (Table 7-3) compares the relative rate of cracking of a 1 1 mixture of n-hexane (molecular diameter 0.49 nm) and 3-methylpentane (molecular diameter 0.56 nm). [Pg.245]


See other pages where Methylpentanes, catalytic cracking is mentioned: [Pg.184]    [Pg.243]    [Pg.837]    [Pg.481]    [Pg.225]    [Pg.329]    [Pg.252]    [Pg.210]    [Pg.297]    [Pg.219]   
See also in sourсe #XX -- [ Pg.183 ]




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