摘要:
Alkenes having a terminal double bond can be isomerized to give alkenes having an internal double bond if alkenes having a terminal double bond or hydrocarbon feedstock having a content of alkenes of this type having a terminal double bond are subjected to treatment, in the presence of hydrogen, over a macroporous or gel-like cation exchanger in the H.sup.+ form which contains 0.001 to 10 g of one or more metals of the VIth and/or VIIth and/or VIIIth sub-group of the periodic system of the elements in elementary form per liter of dry cation exchanger and which has a degree of crosslinking of 2 to 65% and a specific surface area of 5 to 750 m.sup.2 /g of dry exchange resin. The treatment is carried out in the liquid phase at a temperature from 0.degree. to 120.degree. C.
摘要:
Alkyl tert.-alkyl ethers can be cleaved into the underlying alkanols and tert.-olefins in the presence of strongly acidic substances in a column apparatus, the strongly acidic substance being made available at the foot of the column. A particularly advantageous process design results when a water stream is fed below the top column tray in countercurrent to the tert.-olefin flowing upwards and is taken off again from the column above the bottom circulation; in the case of using an insoluble, strongly acidic substance, the latter is located in a catalyst bed at the foot of the column, and the alkyl tert.-alkyl ether is preferably fed in between the catalyst bed and the bottom circulation evaporator.
摘要:
Tert.-Amyl alcohol (TAA) can be prepared in an advantageous manner by hydrating of i-amylenes on an acid cation exchanger by carrying out the reaction in the vicinity of the boiling point of the i-amylenes under the appropriate reaction pressure. A higher content of TAA is thereby obtained in the reaction mixture.
摘要:
Tert.-olefins are obtained in high purity by cleavage of their alkyl ethers, when the catalysts used for this purpose are styrene/divinylbenzene resins which contain sulphonic acid groups and have a macroporous structure and the polymer matrix of which has an internal surface area of at least 400 m.sup.2 /g, a pore volume (porosity) of 0.6-2.5 ml/g and a mean pore diameter of 40-1000 .ANG.. These catalysts show long service lives.
摘要:
The production of 1,2-butadiene in purities of at least 85% becomes possible by means of a process in which a polymerization-inhibitor-containing C4 hydrocarbon fraction is subjected to at least one fractional distillation.
摘要:
Cyclopentane and/or cyclopentene and, if desired, isopentane can be obtained by distillative separation from a pre-benzene fraction or a C5 fraction which has in each case being partially hydrogenated to remove acetylene compounds and diolefins, wherein a) in a first fractional distillation, low boilers are removed as first top product and, either b1) the first bottom product is fed to a second fractional distillation and there cyclopentene is taken off as second top product and cyclopentane and higher-boiling hydrocarbons are taken off as second bottom product and this second bottom product is separated into cyclopentene and higher boilers in a third fractional distillation, or b2) the first bottom product is subjected to a catalytic hydrogenation and subsequently, in a fractional distillation, separated into cyclopentane as top product and higher boilers as bottom product, or b3) the first bottom product is subjected to a fractional distillation to separate off the relatively high boilers as bottom product and the top product is subjected to a catalytic hydrogenation to form cyclopentene.
摘要:
Cyclopentane and/or cyclopentene and, if desired, isopentane can be obtained by distillative separation from a pre-benzene fraction or a C5 fraction which has in each case being partially hydrogenated to remove acetylene compounds and diolefins, wherein a) in a first fractional distillation, low boilers are removed as first top product and, either b1) the first bottom product is fed to a second fractional distillation and there cyclopentene is taken off as second top product and cyclopentane and higher-boiling hydrocarbons are taken off as second bottom product and this second bottom product is separated into cyclopentene and higher boilers in a third fractional distillation, or b2) the first bottom product is subjected to a catalytic hydrogenation and subsequently, in a fractional distillation, separated into cyclopentane as top product and higher boilers as bottom product, or b3) the first bottom product is subjected to a fractional distillation to separate off the relatively high boilers as bottom product and the top product is subjected to a catalytic hydrogenation to form cyclopentene.