Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C7/00—Purification; Separation; Use of additives
  • C07C7/148—Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound
  • C07C7/163—Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound by hydrogenation
  • C07C7/167—Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound by hydrogenation for removal of compounds containing a triple carbon-to-carbon bond

Definitions

• the invention relates to a process for the hydrogenation of phenyl acetylene in a styrene- containing medium with the aid of a catalyst .
• Styrene is often polymerized to polystyrene.
• the phenyl acetylene causes undesirable side reactions during the polymerization, such as cross-linking of the polymer chains. It is therefore of importance to keep the phenyl acetylene content of the styrene-containing medium as low as possible.
• the aim of the invention is to provide a catalyst which does not present said drawback or only to a lesser extent.
• the invention is characterized in that the catalyst is a supported nickel catalyst with a nickel content of 10-25 wt.%.
• a nickel catalyst is much less sensitive to impurities and thus has a much longer service life. This is all the more surprising in that a person skilled in the art, relying on his knowledge of catalysts, would not be likely to opt for a nickel catalyst instead of a palladium catalyst, since a nickel catalyst normally has a lower activity and selectivity than a palladium catalyst in the conversion of acetylenes to alkenes (see for instance J.A. Moulijn, P.W.N.M. van Leeuwen and R.A.
• nickel catalyst applied according to the invention is a supported nickel catalyst. Examples - 3 -
• suitable carrier materials are: silica, - , ⁇ - and y-alumina, zeolites, carbon and oxidic carriers, such as for instance magnesium oxide, titanium oxide and zirconium oxide. Mixtures of different carrier materials can also be used.
• ⁇ - and y- alumina, silica or carbon are used as carrier material.
• ⁇ - or y-alumina is an inert carrier material with a large total surface area and a good poor volume distribution.
• the nickel catalyst is synthesized for instance in the following way.
• the nickel is applied onto the carrier material by impregnating it with a solution of nickel salts. Water is commonly used as solvent.
• the impregnated carrier material is dried and subsequently calcinated at elevated temperature.
• the nickel oxide thus obtained is then activated on the carrier material through a treatment with hydrogen at elevated temperature.
• a high degree of dispersion of the nickel on the carrier results in a catalyst with a large catalytically active surface area. The higher the catalytically active surface area in the catalyst, the better the phenyl acetylene is hydrogenated.
• the nickel content of the nickel catalyst is kept as low as possible.
• a nickel catalyst with a higher nickel content is more expensive and when the nickel content becomes higher, the dispersion of the nickel in the catalyst is worse.
• the nickel content of the catalyst is - 4 -
• Nickel catalysts are commercially available with for instance 10, 15 or 20 wt.% of nickel.
• the nickel content of the nickel catalyst preferably is 11 to 25 wt.%. Most preferably the nickel content of the catalyst is more than 11 and less or equal to 20 wt.%.
• the catalyst can also contain minor amounts of other compounds which enhance the activity and selectivity of the catalyst.
• examples of such compounds are: chromium, gold, rhodium and ruthenium.
• the catalyst can also be modified with sulphur-containing compounds.
• the nickel catalyst When its activity in the hydrogenation of phenyl acetylene has declined strongly, the nickel catalyst can be regenerated. Regeneration is effected for instance by treating the contaminated catalyst with steam and air at a high temperature, for instance 300 to 350°C, followed by reduction with hydrogen at the same temperature. If the catalyst is lightly contaminated it can also be regenerated by merely treating it with hydrogen at an elevated temperature of 100-300 °C.
• cracked petrol When naphtha, gas condensates and LPG are cracked, cracked petrol is formed.
• This cracked petrol mainly contains aliphatic and aromatic compounds with 6-9 carbon atoms, including 1-50 wt.% of styrene. Fractionation of this cracked petrol yields a C8 fraction which contains 30-70 wt.% of styrene. When this C8 fraction is extracted with a solvent and then distilled, a styrene-rich fraction is obtained which may contain more than 95 wt.% of styrene.
• petrol, the C8 fraction as well as the styrene-rich fraction can be used as styrene-containing medium.
• a styrene-containing medium can also be obtained by means of chemical synthesis. Alkylation of benzene with ethene gives ethyl benzene, which through dehydrogenation can be converted into a styrene- containing medium which besides styrene can also contain ethyl benzene and phenyl acetylene.
• the invention is not restricted, however, to the hydrogenation of phenyl acetylene in the above- mentioned styrene-containing media.
• Styrene-containing media which have been obtained in another way can also be employed.
• the styrene-containing media can comprise up to 99.99 wt.% of styrene.
• the styrene-containing medium preferably comprises more than 30 wt.% of styrene.
• the styrene-containing medium is a C8 hydrocarbon fraction which comprises more than 30 wt.% of styrene.
• phenyl acetylene in the styrene-containing medium it is preferred for all phenyl acetylene in the styrene-containing medium to be converted to styrene or ethyl benzene, with a limited amount of phenyl acetylene or styrene being hydrogenated to ethyl benzene.
• the phenyl acetylene content of a styrene- containing medium is normally between 0.01 and 5 wt.% relative to the styrene present in the styrene- containing medium. During the hydrogenation process according to the invention this content is reduced. - 6 -
• Said content is preferably reduced to less than 100 ppm, by particular preference to less than 10 ppm in the styrene-containing medium.
• the process for the hydrogenation of phenyl acetylene in a styrene-containing medium is carried out in a reactor.
• the catalyst on a support is present in the reactor.
• the reactor is fed with the styrene- containing medium and hydrogen gas .
• the hydrogen gas can optionally have been diluted with another, inert gas such as for instance nitrogen gas.
• the styrene- containing medium and the hydrogen gas can be mixed before being fed to the reactor.
• the reactor can be operated as a two-phase or as a three-phase reactor. If the reactor is operated as a two-phase reactor, then the hydrogen gas that is required for the hydrogenation of the phenyl acetylene is fully dissolved in the styrene-containing medium that is supplied to the reactor. If the reactor is operated as a three-phase reactor the styrene-containing medium and the hydrogen gas are fed in at the bottom of the reactor and the product is obtained at the top of the reactor. It is also possible to supply the styrene-containing medium and the hydrogen gas at the top of the reactor and to recover the product at the bottom of the reactor.
• the reactor can also be operated as a countercurrent reactor, with for instance the hydrogen gas being supplied at the bottom of the reactor and the styrene- containing medium at the top.
• the product is recovered at the bottom of the reactor.
• the styrene-containing medium and the hydrogen gas are supplied at the bottom of the reactor, because there is less backmixing then and thus less styrene and phenyl acetylene react further to form ethyl benzene .
• the nickel catalyst is preferably present in a fixed bed in the reactor.
• the styrene-containing medium and the hydrogen gas are contacted with this fixed bed.
• a fixed bed is a bed of solid catalyst parts that can have different shapes and can be, for instance, granules, pellets, extrudates, spheres, triloops and qaudruloops .
• the fixed bed can also consist of a monolith or of miniliths.
• the hydrogen pressure in the reactor is usually between 0 and 300.10 Pa overpressure, preferably between 0 and 50.10 Pa overpressure. Preferably a low pressure is applied, because then the reactor does not have to have a thick wall and is therefore less costly.
• the temperature is usually between 0 and 100 °C, preferably between 15 and 50 °C . If the temperature rises above 50 °C, polymerization of styrene occurs during the reaction.
• the process according to the invention is preferably carried out with a hydrogen : phenyl acetate molar ratio ⁇ 1. By preference this molar ratio is between 1 and 10. For commercial -scale applications this molar ratio is preferably between 1 and 4. The molar ratio is kept as low as possible in order to prevent conversion of styrene and phenyl acetylene into - 8 -
• the average residence time of the styrene- containing medium in the reactor should not be too long, because then more styrene and/or phenyl acetylene react (s) further to ethyl benzene.
• the average residence time should not be too short either, because then the degree of conversion of phenyl acetylene to styrene is too low.
• a measure for the average residence time is the liquid hourly space velocity (LHSV) .
• the process according to the invention is usually carried out with a LHSV of between 0.1 and 100 per hour, preferably between 1 and 10 per hour.
• a reactor with a capacity of 1 m was completely filled with a fixed bed consisting of a nickel catalyst on f3-alumina.
• the catalyst contained 15 wt . % of nickel .
• a C8 fraction comprising 50 wt.% of styrene, 8 wt.% of ethyl benzene and 0.8 wt.% of phenyl acetylene was supplied to the bottom of this reactor.
• Hydrogen gas was also supplied to the bottom of the reactor, the hydrogen gas : phenyl acetylene molar ratio being kept between 2 and 3.
• the LHSV was 4 h " and the contact time was 15 minutes. Further data of the reaction are presented in Table 1. The data were registered after different - 9 -
• Comparative Example A In the reactor of example I a hydrogenation reaction was carried out with a palladium catalyst instead of a nickel catalyst. A palladium catalyst on y-alumina containing 0.2 wt.% of palladium was used.
• Example I after regeneration.
• the catalyst was regenerated by treating it with steam and air at 300 °C, followed by reduction with hydrogen at the same temperature .
• the LHSV was 6 hr "1 and the contact time was
• ⁇ T difference between the inlet and the outlet temperature
• a 95 ml reactor was filled with a fixed bed of 70 ml consisting of nickel catalyst on ⁇ -alumina. - 11 -
• the catalyst contained 15 wt.% of nickel.
• Example III was repeated, using a nickel catalyst on ⁇ -alumina containing 20 wt.% of nickel instead of 15 wt.%.
• the inlet temperature was 30 °C .
• the other reaction conditions were the same as in Example III.
• Hydrogen gas was supplied via the reactor bottom, with a varying hydrogen gas / phenyl acetylene molar ratio, as indicated in Table 2. From Table 2 it appears that at a higher nickel content of the catalyst the same degree of conversion of phenyl acetylene is obtained with a lower hydrogen / phenyl acetylene molar ratio. From this example it also appears that when the hydrogen / phenyl acetylene molar ratio is too high, styrene is also hydrogenated. 12
• Example III was repeated at elevated temperature and with a LHSV of 5.5 hr " .
• a temperature of 70 °C the conversion of phenyl acetylene was 94% at the start of the experiment. After 5 days the conversion of phenyl acetylene had declined to 30%.

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• Analytical Chemistry (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Water Supply & Treatment (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
• Catalysts (AREA)
• Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

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