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Cycloalkanes pyrolysis product

When no reforming process is carried out in the pyrolysis of PP, 90.50% of the gasoline fraction in the products is olefin, and the yield fractions of isomerized paraffins, cycloalkanes and aromatics are very low. The gasoline has a RON of no more than 80 and is very unstable [99]. However, after reforming and fractionation [100], the results improved significantly, as shown in Table 28.11. Two kinds of molecular sieve catalysts were adopted for the process. [Pg.749]

Endoboron Compounds from CycloaU tboranes Cycloalkylboranes will also form heterocyclics by pyrolysis 24,67). Since cycloalkanes cleave readily at fairly low temperatures (ca. 180° C), cycliza-tion proceeds smoothly at 200° C. It is absolutely essential that the cyclic ring be large enough. Tricyclohexylborane does not form 7-borabicydo-[2.2.1]heptane instead, polymeric boron-containing products are formed and volatile materials evolved. [Pg.288]

Ethene (ethylene) can serve as a case study for the significance of alkenes in industrial chemistry. This monomer is the basis for the production of polyethene (polyethylene), millions of tons of which are manufactured in the United States annually. The major source of ethene is the pyrolysis of petroleum, or hydrocarbons derived from natural gas, such as ethane, propane, other alkanes, and cycloalkanes (Section 3-3). [Pg.522]


See other pages where Cycloalkanes pyrolysis product is mentioned: [Pg.182]    [Pg.919]    [Pg.231]    [Pg.283]    [Pg.919]    [Pg.919]    [Pg.237]    [Pg.120]    [Pg.291]   


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Cycloalkan

Cycloalkanes

Pyrolysis products

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