EP1353749A2 - Catalyseur destine a etre utilise pour produire un ester d'acide carboxylique aliphatique inferieur, procede de production dudit catalyseur et procede de production d'un ester d'acide carboxylique aliphatique inferieur a l'aide dudit catalyseur - Google Patents

Catalyseur destine a etre utilise pour produire un ester d'acide carboxylique aliphatique inferieur, procede de production dudit catalyseur et procede de production d'un ester d'acide carboxylique aliphatique inferieur a l'aide dudit catalyseur

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Publication number
EP1353749A2
EP1353749A2 EP01963448A EP01963448A EP1353749A2 EP 1353749 A2 EP1353749 A2 EP 1353749A2 EP 01963448 A EP01963448 A EP 01963448A EP 01963448 A EP01963448 A EP 01963448A EP 1353749 A2 EP1353749 A2 EP 1353749A2
Authority
EP
European Patent Office
Prior art keywords
lower aliphatic
acid
aliphatic carboxylic
carboxylic acid
catalyst
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP01963448A
Other languages
German (de)
English (en)
Inventor
Etsuko C/O OITA PLANT SHOWA DENKO K.K. KADOWAKI
Kousuke C/O OITA PLANT SHOWA DENKO K.K. NARUMI
Hiroshi C/O OITA PLANT SHOWA DENKO K.K. UCHIDA
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Resonac Holdings Corp
Original Assignee
Showa Denko KK
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from JP2000271416A external-priority patent/JP2002079089A/ja
Application filed by Showa Denko KK filed Critical Showa Denko KK
Publication of EP1353749A2 publication Critical patent/EP1353749A2/fr
Withdrawn legal-status Critical Current

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Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/14—Phosphorus; Compounds thereof
    • B01J27/186—Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J27/188—Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium with chromium, molybdenum, tungsten or polonium
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00—Preparation of carboxylic acid esters
    • C07C67/04—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides onto unsaturated carbon-to-carbon bonds

Definitions

  • the present invention relates to a catalyst for use in producing a lower aliphatic carboxylic acid ester from a lower olefin and a lower aliphatic carboxylic acid, a process for producing the catalyst, and a process for producing a lower aliphatic carboxylic acid ester using the catalyst.
  • the present invention relates to a catalyst, containing a specific heteropolyacid, which is used in a process for producing a lower aliphatic carboxylic acid ester by esterifying a lower aliphatic carboxylic acid with a lower olefin, wherein the catalyst is contacted with a gas containing at least one member selected from the group consisting of water, a lower aliphatic carboxylic acid and a lower aliphatic alcohol before the reaction; a process for producing the catalyst; and a process for producing a lower aliphatic carboxylic acid ester using the catalyst.
  • a corresponding ester can be produced from a lower aliphatic carboxylic acid and an olefin.
  • a catalyst comprising a heteropolyacid and/or a heteropolyacid salt is known to act effectively in this reaction. Specific examples of such a catalyst - ⁇
  • JP-A-5-294894 discloses a catalyst obtained by loading at least one heteropolyacid selected from the group consisting of lithium, copper, magnesium and gallium salts of heteropolyacids on a support and it is revealed that although the method disclosed in JP-A-5-170698, of contacting a catalyst with water and an organic carboxylic acid or an organic carboxylic acid ester in a gas phase before performing the reaction, is not used, the catalyst can exhibit initial activity equal thereto or higher and can maintain the activity.
  • the object of the present invention is to provide a catalyst, for use in producing a lower aliphatic carboxylic acid ester from a lower olefin and a lower aliphatic carboxylic acid, which exhibits high initial activity and high space time yield, ensures a catalyst life long enough to endure practice in industry and can reduce the production of by-products; a process for producing the catalyst; and a process for producing a lower aliphatic carboxylic acid ester using the catalyst.
  • the present inventors have made extensive investigations for a catalyst not only capable of exhibiting high initial activity and sufficiently long catalyst life but also reduced in the production of by- products during the reaction of a lower olefin with a lower aliphatic carboxylic acid in a gas phase to produce a lower aliphatic carboxylic acid ester.
  • a neutralized salt of heteropolyacid is not used as the catalyst, when a specific step is provided in the preparation of the heteropolyacid catalyst, the reduction of activity can be prevented.
  • the present invention has been accomplished based on this finding.
  • it is revealed that the production of by-products harmful to the catalyst, such as butene and aldehyde, can be greatly reduced.
  • the present invention has also been accomplished based on this finding.
  • the present invention (I) is a catalyst, for use in producing a lower aliphatic carboxylic acid ester, which is used in reacting a lower olefin with a lower aliphatic carboxylic acid in a gas phase to produce a lower aliphatic carboxylic acid ester, wherein the process for producing the catalyst comprises the following first and second steps: First Step a step of loading one or more heteropolyacid on a support to obtain a heteropolyacid supported catalyst; and Second Step a step of contacting the heteropolyacid supported catalyst, obtained in the first step, with a gas containing at least one member selected from the group consisting of water, a lower aliphatic carboxylic acid and a lower aliphatic alcohol to obtain a catalyst for use in producing a lower aliphatic carboxylic acid ester.
  • the present invention (II) is a process for producing a catalyst, for use in producing a lower aliphatic carboxylic acid ester, the catalyst being used in reacting a lower olefin with a lower aliphatic carboxylic acid in a gas phase to produce a lower aliphatic carboxylic acid ester, wherein the process for producing the catalyst comprises the following first and second steps: First Step a step of loading one or more heteropolyacid on a support to obtain a heteropolyacid supported catalyst; Second Step a step of contacting the heteropolyacid supported catalyst obtained in the first step with a gas containing at least one member selected from the group consisting of water, a lower aliphatic carboxylic acid and a lower aliphatic alcohol to obtain a catalyst for use in producing a lower aliphatic carboxylic acid ester.
  • the present invention (III) is a process, for producing a lower aliphatic carboxylic acid ester, comprising reacting a lower olefin with a lower aliphatic carboxylic acid in a gas phase in the presence of the catalyst for use in producing a lower aliphatic carboxylic acid ester of the present invention (I).
  • the present invention (IV) is a process, for producing a lower aliphatic carboxylic acid ester, comprising reacting a lower olefin with a lower aliphatic carboxylic acid in a gas phase, wherein the production process comprises the following first to fourth steps: First Step a step of loading one or more heteropolyacid on a support to obtain a heteropolyacid supported catalyst; Second Step a step of filling the heteropolyacid supported catalyst obtained in the first step, into a reactor for use in the reaction of a lower olefin with a lower aliphatic carboxylic acid in a gas phase; Third Step a step of contacting a gas containing at least one member selected from the group consisting of water, a lower aliphatic carboxylic acid and a lower aliphatic alcohol, with the heteropolyacid supported catalyst filled in the reactor; and Fourth Step a step of passing a mixed gas containing a lower olefin and a lower aliphatic carboxylic acid
  • the present invention (I) is a catalyst, for use in producing a lower aliphatic carboxylic acid ester, which is used in reacting a lower olefin with a lower aliphatic carboxylic acid in a gas phase to produce a lower aliphatic carboxylic acid ester, wherein the process for producing the catalyst comprises the following first and second steps: First Step a step of loading one or more heteropolyacid on a support to obtain a heteropolyacid supported catalyst; and
  • Second Step a step of contacting the heteropolyacid supported catalyst obtained in the first step with ' a gas containing at least one member selected from the group consisting of water, a lower aliphatic carboxylic acid and a lower aliphatic alcohol to obtain a catalyst for use in producing a lower aliphatic carboxylic acid ester.
  • the catalyst, for use in producing a lower aliphatic carboxylic acid ester, of the present invention (I) is a catalyst obtained by a production process containing the above-described first and second steps in the production step.
  • the heteropolyacid used in the first step comprises a center element and a peripheral element to which oxygen is bonded.
  • the center element is usually silicon or phosphorus but may comprise an arbitrary element selected from various kinds of atoms belonging to Groups I to XVII of the Periodic Table.
  • center element examples include cupric ion; divalent beryllium, zinc, cobalt and nickel ions; trivalent boron, aluminum, gallium, iron, cerium, arsenic, antimony, phosphorus, bismuth, chromium and rhodium ions; tetravalent silicon, germanium, tin, titanium, zirconium, vanadium, sulfur, tellurium, manganese, nickel, platinum, thorium, hafnium, cerium ions and other rare earth element ions; pentavalent phosphorus, arsenic, vanadium and antimony ions; a hexavalent tellurium ion; and a heptavalent iodide ion, however, the present invention is by no means limited thereto.
  • peripheral element include tungsten, molybdenum, vanadium, niobium and tantalum, however, the present invention is by no means limited thereto.
  • heteropolyacids are also known as "polyoxo- anions", “polyoxometallic salts” or “metal oxide clusters”.
  • polyoxo- anions polyoxometallic salts
  • metal oxide clusters metal oxide clusters.
  • Keggin, Wells-Dawson or Anderson-Evans-Perloff structures are described in detail in Poly-San no Kagaku, Kikan Kacraku Sosetsu (Chemistry of Polvacid,
  • a heteropolyacid usually has a high molecular weight, for example, a molecular weight of 700 to 8,500, and includes not only monomers but also dimeric complexes thereof.
  • heteropolyacid which can be used as the starting material of the heteropolyacid in the catalyst for use in producing a lower aliphatic carboxylic acid ester of the present invention (I) include:
  • the present invention is by no means limited thereto.
  • preferred are tungstosilicic acid, tungstophosphoric acid, molybdo- phosphoric acid, molybdosilicic acid, vanadotungstosilicic acid and vanadotungstophosphoric acid, and more preferred are tungstosilicic acid, tungstophosphoric acid, vanadotungstosilicic acid and vanadotungstophosphoric acid.
  • the synthesis method for these heteropolyacids is not particularly limited and any method may be used.
  • the heteropolyacid may be obtained by heating an acidic aqueous solution containing a salt of molybdic acid or tungstic acid and a simple oxygen acid of hetero atom or a salt thereof (pH: about 1 to 2).
  • a method of crystallizing and separating the compound in the form of a metal salt may be used.
  • Specific examples thereof include those described in Shin Jikken Kagaku Koza 8, Muki Kagoubutsu no Gosei t ill ) (New Experimental Chemistry Course 8, Synthesis of Inorganic Compounds (III) ) , 3rd ed., page 1413, edited by Nippon Kagaku Kai, issued by Maruzen (March 20, 1984), however, the present invention is not limited thereto.
  • the Keggin structure of the heteropolyacid synthesized may be identified by chemical analysis or by X-ray diffraction or UV or IR measurement.
  • the heteropolyacid has a relatively high solubility in a polar solvent such as water and other oxygen- containing solvents, and the solubility can be controlled by appropriately selecting the counter ion.
  • the heteropolyacid as a catalytic activity component is loaded on a support.
  • a substance which can be used as the support is not particularly limited and a porous substance commonly used as a support may be used. Specific examples thereof include those comprising silica, diatomaceous earth, montmorillonite, titania, activated carbon, alumina and silica alumina, preferably silica and titania.
  • the support is also not limited on the shape thereof and may be a powder or in a spherical, pellet-like or any other arbitrary shape. The shape is preferably a sphere or a pellet.
  • the particle size is not particularly limited and in the case of a fixed bed reactor, the particle size is preferably from 2 to 10 mm, more preferably from 3 to 7 mm, and in the case of a fluidized bed reactor, the particle size is preferably from powder to 5 mm, more preferably from powder to 2 mm, though this varies depending on the reactor.
  • the support is most preferably a spherical or pellet-like siliceous support.
  • the source or amount of the elements previously contained in the support can be measured by chemical analysis such as inductively coupled plasma emission spectrometry (hereinafter simply referred to as "ICP"), a fluorescent X-ray spectrometry or an atomic absorption spectrometry.
  • ICP inductively coupled plasma emission spectrometry
  • a fluorescent X-ray spectrometry or an atomic absorption spectrometry.
  • the method for loading a solution or suspension of heteropolyacid on a support in the first step of the catalyst, for producing a lower aliphatic carboxylic acid ester of the present invention (I), is not particularly limited and a known method may be used.
  • the catalyst may be prepared by dissolving a heteropolyacid in a distilled water corresponding to the liquid absorption amount of the support used and impregnating the solution into a support.
  • the catalyst may be prepared using an excess aqueous solution by impregnating it into a support while appropriately Cn • a cd
  • contact means to contact the heteropolyacid supported catalyst obtained in the first step with a gas containing at least one member selected from the group consisting of water, a lower aliphatic carboxylic acid and a lower aliphatic alcohol.
  • the method for the contact is not particularly limited and for example, the following methods may be used: (a) a method of placing the heteropolyacid supported catalyst obtained in the first step in an atmosphere of a gas containing at least one member selected from the group consisting of water, a lower aliphatic carboxylic acid and a lower aliphatic alcohol; (b) a method of passing a gas containing at least one member selected from the group consisting of water, a lower aliphatic carboxylic acid and a lower aliphatic alcohol through the heteropolyacid supported catalyst obtained in the first step; and (c) a method of passing the heteropolyacid supported catalyst obtained in the first step, through an atmosphere of a gas containing at least one member selected from the group consisting of water, a lower aliphatic carboxylic acid and a lower aliphatic alcohol can be performed.
  • a method of filling the supported catalyst obtained in the first step into a vessel and contacting the gas therewith for example, a method of filling the supported catalyst obtained in the first step into a vessel and contacting the gas therewith, or a method of filling the supported catalyst obtained in the first step into, in place of the vessel, a reactor where the production process of a lower aliphatic carboxylic acid ester is performed later, and contacting the gas therewith before feeding reaction starting materials, may be used.
  • any shape such as vertical type or • ⁇ Cn m 4J ⁇ TJ .
  • the lower aliphatic carboxylic acid in a gas containing at least one member selected from the group consisting of water, a lower aliphatic carboxylic acid and a lower aliphatic alcohol used in the second step is preferably a lower aliphatic carboxylic acid having from 1 to 6 carbon atoms. Specific examples thereof include formic acid, acetic acid, propionic acid, n-butyric acid and isobutyric acid. Among these, preferred are acetic acid and propionic acid.
  • the lower aliphatic alcohol in a gas containing at least one member selected from the group consisting of water, a lower aliphatic carboxylic acid and a lower aliphatic alcohol used in the second step is preferably a lower aliphatic alcohol having from 1 to 6 carbon atoms.
  • Specific examples thereof include methanol, ethanol, 1- propanol, 2-propanol, 1-butanol and 2-butanol. Among these, preferred are methanol, ethanol and n-propanol.
  • the composition of the gas containing at least one member selected from the group consisting of water, a lower aliphatic carboxylic acid and a lower aliphatic alcohol used in the second step is not particularly limited, and water, a lower aliphatic carboxylic acid and a lower aliphatic alcohol can be mixed in an arbitrary ratio.
  • the composition of the gas may be constant from the beginning to the end of contacting or may be changed according to the contacting time or the stage of contacting.
  • the gas containing at least one member' selected from the group consisting of water, a lower aliphatic carboxylic acid and a lower aliphatic alcohol used in the second step is more preferably water alone or a mixed gas of water and acetic acid, still more preferably a mixed gas of water and acetic acid because the effect can be provided within a short time.
  • the gas hourly space velocity (hereinafter referred to as the "GHSV") of the gas which is the speed of feeding the gas in performing the contact with a gas containing at least one member selected from the group consisting of water, a lower aliphatic carboxylic acid and a lower aliphatic alcohol in the second step, is not particularly limited.
  • the GHSV is preferably from 100 to 7,000 hr "1 , more preferably from 300 to 3,000 hr "1 .
  • the contacting may also be performed by feeding a constant amount of the gas and enclosing it in a vessel.
  • the contacting time is not particularly limited, however, it is preferably from 0.5 to 200 hours, more preferably from 0.5 to 100 hours, and most preferably from 0.5 to 50 hours.
  • the optimal time varies depending on the composition and concentration of the gas, the temperature and pressure at the contacting, and the catalyst component.
  • the effect of the second step may not be fully brought out, whereas if the contacting time is prolonged, the effect is liable to increase but even if the contacting time is prolonged to exceed 200 hours, the effect does not increase any more, moreover, in the case where gas is contacted in a flowing state, the amount of the gas used increases and this is not preferred in view of the profitability.
  • the first step and the second step may be performed either continuously or completely independently. More specifically, for example, a catalyst for use in producing a lower aliphatic carboxylic acid ester, which is obtained by purchasing a heteropolyacid catalyst passed through the first step and then subjecting it to the second step, is of course included in the scope of the catalyst for use in producing a lower aliphatic carboxylic acid ester of the present invention (I).
  • the present invention (II) is described below.
  • the present invention (II) is a process for producing a catalyst for use in producing a lower aliphatic carboxylic acid ester, the catalyst being used in reacting a lower olefin with a lower aliphatic carboxylic acid in a gas phase to produce a lower aliphatic carboxylic acid ester, wherein the production process comprises the following first and second steps: First Step a step of loading one or more heteropolyacid on a support to obtain a heteropolyacid supported catalyst; and Second Step a step of contacting the heteropolyacid supported catalyst obtained at the first step with a gas containing at least one member selected from the group consisting of water, a lower aliphatic carboxylic acid and a lower aliphatic alcohol to obtain a catalyst for use in producing a lower aliphatic carboxylic acid ester.
  • the heteropolyacid and the support used in the first step, the method for loading the heteropolyacid on a support performed in the first step, the method for measuring the amount of heteropolyacid supported, and the preferred amount of heteropolyacid supported on a support are the same as in the present invention (I).
  • the method for contacting the catalyst with a gas containing at least one member selected from the group consisting of water, a lower aliphatic carboxylic acid and a lower aliphatic alcohol performed in the second step, the conditions therefor such as temperature, pressure, GHSV and time, the lower aliphatic carboxylic acid and lower aliphatic alcohol used for the gas, and the compositional ratio of the gas to which water is further added, are also the same as in the present invention (I).
  • First Step A step of loading one or more heteropolyacid on a support to obtain a heteropolyacid supported catalyst.
  • steps which are provided, if desired, include a step of loading a third component so as to more improve the catalytic activity. In such a case, this loading operation may be performed simultaneously with the operation of loading the heteropolyacid in the first step, if possible.
  • the present invention (III) is described below.
  • the present invention (III) is a process for producing a lower aliphatic carboxylic acid ester, comprising reacting a lower olefin with a lower aliphatic carboxylic acid in a gas phase in the presence of the catalyst for use in producing a lower aliphatic carboxylic acid ester, of the present invention (I).
  • the gas phase reaction is not particularly limited in the reaction form and the reaction may be performed in any form such as fixed bed or a fluidized bed.
  • the shape of the support which governs the shape or size of the catalyst may be selected in the range from powder to a compact formed into a size of several mm, according to the reaction form employed.
  • Examples of the lower olefin which can be used in the process for producing a lower aliphatic carboxylic acid ester of the present invention (III), include ethylene, propylene, n-butene, isobutene and a mixture of two or more thereof .
  • the lower aliphatic carboxylic acid is suitably an aliphatic carboxylic acid having from 1 to 4 carbon atoms and specific examples thereof include formic acid, acetic acid, propionic acid, butyric acid, acrylic acid, methacrylic acid, and a mixture of two or more thereof. Among these, preferred are acetic acid, propionic acid and acrylic acid, more preferred is acetic acid.
  • a lower olefin and a lower aliphatic carboxylic acid which is preferably used in the process for producing a lower aliphatic carboxylic acid ester of (III)
  • ethylene and acetic acid ethylene and propionic acid
  • propylene and acetic acid propylene and propionic acid
  • propylene and propionic acid propylene and propionic acid.
  • most preferred is the combination of ethylene and acetic acid.
  • the ratio between the lower olefin and the lower aliphatic carboxylic acid used as the starting materials is not particularly limited.
  • the lower olefin is preferably used 00 CO
  • ether produced as by-products in the reaction may be recycled and used as they are.
  • the present invention (IV) is described below.
  • the present invention (IV) is a process for producing a lower aliphatic carboxylic acid ester, comprising reacting a lower olefin with a lower aliphatic carboxylic acid in a gas phase, wherein the production process comprises the following first to fourth steps:
  • First Step a step of loading one or more heteropolyacid on a support to obtain a heteropolyacid supported catalyst
  • Second Step a step of filling the heteropolyacid supported catalyst obtained in the first step, into a reactor for use in the reaction of a lower olefin with a lower aliphatic carboxylic acid in a gas phase;
  • Third Step a step of contacting a gas containing at least one member selected from the group consisting of water, a lower aliphatic carboxylic acid and a lower aliphatic alcohol, with the heteropolyacid supported catalyst filled in the reactor; and
  • Fourth Step a step of passing a mixed gas containing a lower olefin and a lower aliphatic carboxylic acid through the heteropolyacid supported catalyst after the third step, to obtain a lower aliphatic carboxylic acid ester.
  • the first step is described below.
  • the first step in the process for producing a lower aliphatic carboxylic acid ester of the present invention (IV) is a step of loading one or more heteropolyacid on a support to obtain a heteropolyacid supported catalyst.
  • the catalyst vary depending on the form of the reactor and these are not particularly limited.
  • Specific examples of the reactor include Fig. C «4 «43 "Methanol Contacting Gaseous Phase Reactor” in the item of "4) Fixed catalyst gas phase reactor", described in Kagaku Sochi Binran (Chemical Apparatuses Handbook), 2nd ed., 3rd imp., pp. 905 to 906, edited by Kagaku Kogyo Kyokai, published by Maruzen (February 20, 1980).
  • the third step is described below.
  • the third step in the process for producing a lower aliphatic carboxylic acid ester of the present invention (IV) is a step of contacting a gas containing at least one member selected from the group consisting of water, a lower aliphatic carboxylic acid and a lower aliphatic alcohol, with the heteropolyacid supported catalyst filled in the reactor.
  • the method for contacting the catalyst with a gas containing at least one member selected from the group consisting of water, a lower aliphatic carboxylic acid and a lower aliphatic alcohol performed in the third step, the conditions such as temperature, pressure, GHSV and time, the lower aliphatic carboxylic acid and lower aliphatic alcohol used for the gas, and the compositional ratio of the gas to which water is further added, are the same as in the second step of the present invention (I).
  • the conditions therefor are not particularly limited, and the preferred conditions are considered to vary depending on the form, shape, size or constructive material of the reactor used for the contacting.
  • the contacting may be performed in the conditions described above for the second step of the present invention ( I ) .
  • the fourth step is described below.
  • the fourth step of the present invention (IV) is a step of passing a mixed gas containing a lower olefin and a lower aliphatic carboxylic acid through the heteropolyacid supported catalyst after the third step, to obtain a lower aliphatic carboxylic acid ester.
  • the preferred combinations and ratio in the amounts of the lower olefin and the lower aliphatic carboxylic acid used in the fourth step, the conditions in the practice of the fourth step, such as addition of water, temperature, pressure and GHSV, and the recycling operation mainly of unreacted lower olefin, those in the process for the producing a lower aliphatic carboxylic acid ester of the present invention (III) can be applied.
  • the third step and the fourth step of the present invention (IV) may or may not be clearly distinguished.
  • Examples of the practical embodiment having a clear distinction between those two steps include the case where after judging that the contacting in the third step is finished, the flow of the gas containing at least one member selected from the group consisting of water, a lower aliphatic carboxylic acid and a lower aliphatic alcohol is once stopped or the temperature is further lowered to terminate the third step and, thereafter, the starting material gas containing a lower olefin and a lower aliphatic carboxylic acid is passed as the reaction gas in the fourth step.
  • Examples of practical embodiments not having a clear distinction between those two steps include the case where, after judging that the contacting in the third step is finished, while not once stopping the flow of the gas containing at least one member selected from the group consisting of water, a lower aliphatic carboxylic acid and a lower aliphatic alcohol or by adjusting the temperature to the range suitable for the fourth step to prepare the initiation of reaction, the starting material gas containing a lower olefin and a lower aliphatic carboxylic acid is passed as the reaction gas in the fourth step.
  • the reaction may be performed according to a practical embodiment not having a clear distinction between the third step and the fourth step.
  • the reaction is preferably performed by providing a clear distinction between those two steps.
  • the contacting in the third step is preferably performed using a lower aliphatic carboxylic acid corresponding to the objective ester in the process for producing a lower aliphatic carboxylic acid ester of the present invention (IV).
  • a lower aliphatic carboxylic acid corresponding to the objective ester in the process for producing a lower aliphatic carboxylic acid ester of the present invention (IV) For example, in the case of producing ethyl acetate as the lower aliphatic carboxylic acid ester by applying the process for producing a lower aliphatic carboxylic acid ester of the present invention (IV), one of the preferred practical embodiments is a method of performing the contacting in the third step using a mixed gas of water and acetic.
  • the analysis of metals in the support was performed using a fluorescent X-ray analyzer (PW2404, manufactured by PHILIPS ) . Measurement conditions were such that the atmosphere was helium, the effective diameter was 25.0 mm, and the matrix was 2Si0 2 .
  • the detector and the vaporization chamber were at a temperature of 120 °C, and the column temperature was 65°C and constant.
  • Detector FID (H 2 pressure: 60 kPa, air pressure: 100 kPa) 2. Butene
  • the detector and the vaporization chamber were at a temperature of 130 °C, and the column temperature was elevated from 40 °C to 95 °C at a temperature increasing rate of 40°C/min.
  • the detector and the vaporization chamber were at a temperature of 120 °C, and the column temperature was 65 °C and constant.
  • the analysis was performed using the internal standard method, where the analysis solution was prepared by adding 1 ml of 1,4-dioxane as the internal standard to 10 ml of the reaction solution and 0.4 ⁇ l of the analysis solution was injected.
  • Carrier gas nitrogen (split ratio: 20, column flow rate: 1 ml/min)
  • the detector and the vaporization chamber were at a temperature of 200 °C, and the column temperature was kept at 40°C for 7 minutes from the start of analysis, then elevated to 230 °C at a temperature increasing rate of 10°C/min, and kept at 230 °C for 5 minutes .
  • Support 3 silica gel (Wakogel C-200 , produced by Wako
  • Support 1 was preliminarily dried for 4 hours in a (hot-air type) drier previously adjusted to 110°C. After the preliminary drying, 1 liter of the support was measured on the bulk density using a 1 liter measuring cylinder. Tungstosilicic acid was weighed to the amount shown in Table 1 and after adding thereto 15 ml of pure water, uniformly dissolved. To this impregnating solution, pure water was further added to make the liquid amount shown in Volume of Solution Prepared of Table 1. Thereafter, the preliminarily dried support was weighed to the amount shown in Table 2, added to the impregnating solution and impregnated with the solution while thoroughly stirring.
  • the support impregnated with the solution was transferred to a porcelain dish, air-dried for 1 hour and then dried in a hot-air type drier adjusted to 150 °C for 5 hours. After the drying, the catalyst was transferred to a desiccator and left standing to cool to room temperature. The weight of the thus-obtained catalyst was measured.
  • a pressure-resistant vessel made of SUS316L 50 ml of the catalyst obtained in Preparation Process of Catalyst 1 was filled and then contacted under the contacting conditions shown in Table 3. After the contacting, the vessel was returned to room temperature and the catalyst used for the contacting (hereinafter simply referred to as a "contacted catalyst") was taken out from the vessel.
  • the reduction in activity can be suppressed and when used as a catalyst in producing a lower aliphatic carboxylic acid ester from a lower olefin and a lower aliphatic carboxylic acid, the catalyst can exhibit high initial activity and high space time yield, to ensure a sufficiently long catalyst life in industrial practice, and can reduce the production of by-products .

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Abstract

Catalyseur destiné à être utilisé pour produire un ester d'acide carboxylique aliphatique inférieur, qui peut présenter une forte activité initiale et un rendement élevé de l'espace-temps, ainsi qu'une durée de vie suffisamment longue dans des processus industriels, et en outre réduire la production de sous-produits, procédé de production dudit catalyseur et procédé de production d'un ester d'acide carboxylique aliphatique inférieur à l'aide dudit catalyseur. Ledit catalyseur est produit selon un procédé qui consiste à mettre en contact ce catalyseur avec un gaz contenant au moins un élément sélectionné parmi de l'eau, un acide carboxylique aliphatique inférieur et un alcool aliphatique inférieur.
EP01963448A 2000-09-07 2001-09-05 Catalyseur destine a etre utilise pour produire un ester d'acide carboxylique aliphatique inferieur, procede de production dudit catalyseur et procede de production d'un ester d'acide carboxylique aliphatique inferieur a l'aide dudit catalyseur Withdrawn EP1353749A2 (fr)

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JP2000271416A JP2002079089A (ja) 2000-09-07 2000-09-07 低級脂肪族カルボン酸エステル製造用触媒、該触媒の製造方法、及び該触媒を用いた低級脂肪族カルボン酸エステルの製造方法
JP2000271416 2000-09-07
US23843100P 2000-10-10 2000-10-10
US238431P 2000-10-10
PCT/JP2001/007709 WO2002020158A2 (fr) 2000-09-07 2001-09-05 Catalyseur destine a etre utilise pour produire un ester d'acide carboxylique aliphatique inferieur, procede de production dudit catalyseur et procede de production d'un ester d'acide carboxylique aliphatique inferieur a l'aide dudit catalyseur

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WO2006032843A1 (fr) 2004-09-22 2006-03-30 Bp Chemicals Limited Support de silice, catalyseur hétéropolyacide synthétisé à partir dudit support, et synthèse d’ester employant le catalyseur hétéropolyacide supporté
EP2089156B1 (fr) * 2006-11-22 2022-01-05 Technip E&C Limited Procédé de production d'alcènes à partir d'oxygénats en utilisant des catalyseurs hétéropolyacides supportés
CN103980114B (zh) * 2014-04-14 2016-01-20 武汉强丰新特科技有限公司 一种丙烯酸双环戊二烯酯的制备方法
CN104030919B (zh) * 2014-06-27 2015-11-18 无锡阿科力科技股份有限公司 一种连续法制备(甲基)丙烯酸叔丁酯的工艺方法

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JP3012059B2 (ja) * 1991-11-05 2000-02-21 昭和電工株式会社 低級脂肪酸エステルの製造方法
DE69607536T2 (de) * 1995-08-02 2001-02-08 Bp Chem Int Ltd Estersynthese
DE60109449D1 (de) * 2000-06-27 2005-04-21 Showa Denko Kk Katalysator brauchbar für die herstellung von niedrigem aliphatischem carbonsäureester,verfahren für die herstellung des katalysators und verfahren für die herstellung der niedrigen aliphatischen carbonsäureesster unter verwendung des katalysators

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CN1452511A (zh) 2003-10-29
AU2001284440A1 (en) 2002-03-22
WO2002020158A2 (fr) 2002-03-14
WO2002020158A3 (fr) 2002-06-20
BR0113736A (pt) 2003-07-29

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