Classifications

• • 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
  • C07C67/05—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides onto unsaturated carbon-to-carbon bonds with oxidation
• • 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
  • C07C67/05—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides onto unsaturated carbon-to-carbon bonds with oxidation
  • C07C67/055—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides onto unsaturated carbon-to-carbon bonds with oxidation in the presence of platinum group metals or their compounds
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
  • Y02P20/00—Technologies relating to chemical industry
  • Y02P20/50—Improvements relating to the production of bulk chemicals
  • Y02P20/582—Recycling of unreacted starting or intermediate materials

Definitions

• the invention relates to improved integrated methods of making vinyl acetate monomers from ethane or ethylene using metal oxide catalysts. Description of the Related Art
• lower alkanes C.-C as feed stock to produce value added petrochemicals
• Lower alkanes are low cost and environmentally acceptable because of their low chemical reactivity.
• Vinyl acetate monomer (VAM) is a well-known industrial chemical.
• VAM Vinyl acetate monomer
• the production of VAM from ethylene, oxygen and acetic acid using conventional VAM catalysts is known in the art.
• VAM is typically used as a raw material for vinyl resins such as polyvinyl acetate.
• VAM was previously primarily manufactured from the vapor phase reaction of ethylene, acetic acid and oxygen with a zinc acetate catalyst.
• VAM has been produced from the vapor- phase reaction of ethylene, acetic acid and oxygen, with a palladium catalyst.
• VAM may be made from ethylene wherein the first step involves reacting the ethylene to form acetic acid, followed by a second step of reacting a mixture of the acetic acid and ethylene to form vinyl acetate .
• PCT Patent Publication WO 98/05620 describes the production of acetic acid and/or vinyl acetate from ethylene (or ethane) using a first catalyst active for the oxidation of ethylene to acetic acid and/or active for the oxidation of ethane to acetic acid, ethylene and carbon monoxide, and a second catalyst active for the production of vinyl acetate.
• the patent also describes an additional necessary step for conversion of carbon monoxide to carbon dioxide. This is because carbon monoxide is poisonous to the VAM catalyst .
• U.S. Patent No. 4,188,490 relates to a catalytic oxidation process for the production of mixtures of acetic acid and vinyl acetate comprising the step of contacting a feed mixture containing ethylene, oxygen and water (as steam) with a catalyst composition to provide a mixture of acetic acid and vinyl acetate.
• the catalyst system comprises a palladium metal on a zinc oxide support treated in the presence of a sulfur modifier.
• the method requires the subsequent step of fractional distillation to separate the acetic acid from the vinyl acetate.
• the acetic acid contained in the product mixture is converted in situ to an alkali metal salt such as sodium acetate.
• the method also requires the step of treating the catalyst with the sulfur modifier by, for example, flowing moist air containing S0 2 over the catalyst at 200°C for about one hour.
• vinyl acetate is produced catalytically from ethane feed stocks .
• Another aspect of the invention relates to the production of vinyl acetate from ethylene.
• the catalysts suitable for use in the methods of the invention are active and selective to the desired end product, vinyl acetate.
• the catalytic process for the production of VAM from ethane involves two steps. In the first step, a catalyst (the "first catalyst") is used to provide the function of activation of ethane to ethylene and acetic acid. In the second step, ethylene and acetic acid are further oxidized to VAM in the presence of a conventional VAM catalyst (the "second catalyst").
• Another preferred embodiment relates to a method of forming a stoichiometric mixture of ethylene and acetic acid using the first catalyst, which mixture can be directly fed into a vinyl acetate reactor containing the VAM catalyst without adjustments.
• Yet another preferred embodiment relates to a catalytic method wherein ethylene or ethane is converted to vinyl acetate in a single stage reactor.
• the preferred catalytic methods of the invention do not produce carbon monoxide. This is advantageous because carbon monoxide is not environmentally friendly and can have a significant impact on down stream separation costs, as well as on the poisoning of the VAM catalyst .
• Figure 1 is a schematical representation of a ethane to VAM reaction scheme according to one embodiment of the invention.
• Figure 2 is a schematical representation of a ethane to VAM reaction scheme according to another embodiment of the invention.
• the invention relates to novel methods of producing vinyl acetate.
• the first catalyst is used which provides the dual functions of (a) activation of ethane (or ethane/ethylene) to acetic acid and ethylene and (b) ethylene to acetic acid.
• vinyl acetate is formed through further oxidation of ethylene with acetic acid in the presence of a second catalyst, the VAM catalyst.
• the catalysts of the invention can also be used to provide an optimal feed to a vinyl acetate reactor.
• the catalyst system suitable for the first step of the present invention can be formed from compositions including a catalyst (a) of the formula Mo a V b Nb c Pd d , wherein: a is 1 to 5 ; b is 0 to 0 . 5 ; c is 0 . 01 to 0 . 5 ; and d is 0 to 0.2.
• the numerical values of a, b, c and d represent the relative gram-atom ratios of the elements Mo, V, Nb and Pd, respectively, in the catalyst.
• the elements are preferably present in combination with oxygen in the form of various oxides.
• Another catalyst system, catalyst (b) has a composition comprising the elements Mo, V, Pd, Nb, La, and X (where X is Al, Ga, Si, or Ge) in the form of oxides in the ratio Mo a V b La c Pd d Nb e X f wherein: a is 1 ; b is 0.01 to 0.9; c is > 0 to 0.2; d is > 0 to 0.2. e is > 0 to 0.2; and f is > 0 to 0.3.
• the numerical values of a, b, c, d, e and f represent the relative gram-atom ratios of the elements Mo, V, Pd, La, Nb and X, respectively, in the catalyst.
• the elements are preferably present in combination with oxygen in the form of various oxides .
• catalyst (c) suitable for the invention is formed from a calcined composition of Mo a V b Nb c X d , wherein: X is at least one promoter element selected from the group consisting of: P, B, Hf, Te, and As; A is about 1 to 5;
• d is about 0 to 0.1.
• the numerical values of a, b, c and d represent the relative gram-atom ratios of the elements Mo, V, Nb and X, respectively, in the catalyst.
• the elements are preferably present in combination with oxygen in the form of various oxides .
• the first catalyst (catalysts (a) or (b) or (c) or mixtures thereof) and methods of making the first catalyst are set forth in copending U.S. Application Serial No. 08/932,075 (Attorney Docket No. 582815-2060), filed September 17, 1997, entitled "Catalysts for the Oxidation of Ethane to Acetic Acid, Processes of Making the Same and Processes of Using the Same"; U.S. Patent Application Serial No. 08/997,913 (Attorney Docket No.
• One broad aspect of the invention relates to the production of vinyl acetate from ethane, ethylene or mixtures of ethane and ethylene.
• the method utilizes a first catalyst ((a) or (b) or (c) or mixtures thereof) providing the functions of activation of ethane to acetic acid and ethylene and further oxidation of ethylene with acetic acid to vinyl acetate using a conventional VAM catalyst such as a Pd/Al catalyst.
• a first catalyst ((a) or (b) or (c) or mixtures thereof) providing the functions of activation of ethane to acetic acid and ethylene and further oxidation of ethylene with acetic acid to vinyl acetate using a conventional VAM catalyst such as a Pd/Al catalyst.
• a conventional VAM catalyst such as a Pd/Al catalyst
• the methods of the invention produce vinyl acetate with zero (or nondetectable) or insignificant production of carbon monoxide.
• one preferred aspect of the invention relates to a method which employs a catalyst designed in such way that it does not produce any CO, which saves the treatment step of converting CO to C0 2 .
• One embodiment of the invention comprises reacting ethane with oxygen and water (e.g. steam) in the presence of a first catalyst ( (a) or (b) or (c) or mixtures thereof) to form a mixture containing ethylene and acetic acid which is then reacted to form vinyl acetate.
• a first catalyst (a) or (b) or (c) or mixtures thereof) to form a mixture containing ethylene and acetic acid which is then reacted to form vinyl acetate.
• the raw material used as the source for the ethane or ethylene/ethane can be a gas stream, which preferably contains at least five volume percent of ethane/ethylene.
• the gas can also contain minor amounts of the C 3 -C 4 alkanes and alkenes, preferably less than five volume percent of each.
• the gas stream can also contain major amounts, preferably more than five volume percent, of nitrogen, carbon dioxide, and water in the form of steam.
• the reaction mixture useful in carrying out the process is generally from 5 to 50 moles % of ethane, 5 to 50 moles % of molecular oxygen either as pure oxygen or in the form of air, and optionally 2 to 50 moles % of water in the form of steam.
• the amount of oxygen present may be a stoichiometric amount, or lower, of the hydrocarbons in the feed.
• Other gases may be used as reaction diluents or heat moderators such as helium, nitrogen, and carbon dioxide .
• the gaseous components of the reaction mixture are preferably uniformly admixed prior to being introduced into the reaction zone.
• the components may be preheated, individually or after being mixed, prior to being introduced into the reaction zone.
• the first reaction zone containing the first catalyst ( (a) or (b) or (c) or mixtures thereof) , generally has a pressure of from 15 to 500 psi, preferably from 150 to 350 psi; a temperature of from about 100°C to about 450°C, preferably from 200°C to 350°C, more preferably from 250°C to 300°C; a contact time between the reaction mixture and the catalyst of from about 2 seconds to about 100 seconds, preferably from 5 seconds to 30 seconds; and a space hourly velocity of from about 50 to about 50,000 h "1 , preferably from 100 to 10,000 h "1 and most preferably from 200 to 3,000 h "1 .
• the process occurs in two stages.
• a mixture comprising ethane or ethylene, oxygen or a compound capable of providing oxygen and water (e.g., steam) is reacted to form a mixture containing ethylene, acetic acid, oxygen and water (e.g., steam).
• the product mixture of the first stage is then fed into the second stage and reacted to produce vinyl acetate.
• the feed from the first stage may be adjusted prior to being introduced into the second stage.
• the oxygen, ethylene and acetic acid concentration may be adjusted to optimize the catalytic reaction.
• the first stage of the process produces a stoichiometric composition of acetic acid and ethylene as a feed for the second stage .
• adjustments of the feed for the second reactor are not required as the mixture produced in the first stage can be directly fed into the second stage.
• a dual-function catalyst can be used in the first stage to provide the feed stock for the second stage, which may contain a conventional Pd/Al VAM catalyst or any catalyst suitable for converting the feed stock of acetic acid and ethylene to VAM.
• VAM can also be directly produced from only ethane, oxygen and water without additional components since the outlet of the first reactor may be optimized to contain a stoichiometric mixture of acetic acid, - 1 2 -
• ethylene and oxygen which is the feed mixture for the second reactor.
• the temperature and pressure of the feed from the first stage are also not adjusted prior to the second stage .
• the output from either the first or second stage is recycled into the same or an earlier stage.
• the output from stage 1 may be recycled into stage 1 or the output from stage 2 may be recycled into stage 1 and/or stage 2.
• the reaction zone comprises multiple stages of bilayered catalyst consisting of layers of a first catalyst ( (a) or (b) or (c) or mixtures thereof) according to the invention and a second conventional vinyl acetate catalyst.
• the first catalyst converts ethane to a mixture of acetic acid and ethylene, preferably to an optimal mixture
• the second catalyst converts the ethylene/acetic acid to vinyl acetate in a single reaction zone .
• one preferred embodiment relates to a process carried out in a single stage with all the reactants being supplied as a single feed with unreacted initial reactants being recycled.
• multiple stage addition of oxygen to the reactor with an intermediate hydrocarbon feed can also be used. This may improve productivity to vinyl acetate and avoid potentially hazardous conditions.
• Two possible integrated schemes using the first catalyst and the second VAM catalyst for direct production of VAM from ethane or ethane/ethylene mixtures without producing carbon monoxide are shown in Figures 1 and 2.
• the liquid stream from gas/liquid separation unit 2 goes to distillation unit 3, where acetic acid is separated from water or the liquid stream from gas/liquid separation unit 2 can directly go to VAM reactor 5 containing a conventional VAM catalyst (CAT-B) .
• VAM reactor 5 containing a conventional VAM catalyst (CAT-B) .
• the treated gases consisting of ethane, ethylene and oxygen and the liquid stream consisting of acetic acid or acetic acid and water are fed to VAM reactor 5 to produce VAM, C0 2 and unreacted ethane, ethylene and acetic acid.
• the effluent of VAM reactor 5 is then fed to gas liquid separation unit 6 where gases including ethane, ethylene and C0 2 are separated, partially purged to control the build up of non reacting species in purge unit 8 and recycled back to partial oxidation reactor 1.
• the liquids are sent to distillation unit 7 for recovery of VAM. Acetic acid or unreacted acetic acid is recycled back to VAM reactor 5.
• FIG. 2 is a schematical representation of reaction scheme B according to another embodiment of the invention.
• the partial oxidation reactor 21 containing the first catalyst (CAT- A) converts fresh and recycled ethane or ethane/ethylene with oxygen into ethylene, acetic acid and carbon dioxide.
• the effluent of reactor 21 is fed to VAM reactor 23 containing the VAM catalyst (CAT-B) via optional heat exchanger 22, which allows adjustment of the temperature of the feed to VAM reactor 23.
• the two catalysts CAT-A and CAT-B can be in one reactor in the form of a physical mixture or in alternating layer form. Additional amounts of gases to VAM reactor 23, such as ethylene, acetic acid, and oxygen may be added depending upon the process conditions.
• the effluent from VAM reactor 23 is fed to gas/liquid separation unit 24, where gases including C0 2 , C 2 H 4 , and C 2 H 6 are separated from liquid VAM, acetic acid and water.
• the gas streams from gas/liquid separation unit 24 are recycled via carbon dioxide removal unit 25 to reactor 21.
• the gas streams can also be recycled to reactor 21 without the absorption unit 25, as the catalyst CAT-A in the reactor 21 is not affected by the presence of carbon dioxide. Further, a specific amount of carbon dioxide also enhances the performance of the catalyst CAT-A. Gases are partially purged to control the build up of non reacting species in purge unit 27.
• Liquid stream from separator unit 24 is fed to distillation unit 26 where acetic acid is separated from VAM and water and is optionally recycled to reactor 23 for make up or can be recovered.
• VAM goes to a recovery unit and H 2 0 is recycled to reactor unit 21 for enhancement of acetic acid and selectivity.
• Catalytic oxidation processes using a first catalyst were carried out in a tubular reactor under the following conditions . All experiments were run at the temperatures set forth below ranging from 260°C to 286°C, at a pressure of about 200 psig.
• Reaction products were analyzed on-line by gas chromatography.
• Oxygen, nitrogen and carbon monoxide were analyzed using a 3 mm by 3 mm column of 13X molecular sieve.
• Carbon dioxide, ethane, ethylene and water were analyzed using a 1.8 m by 3mm column packed with material sold under the name HAYASEPTMQ.
• Acetic acid was analyzed using a 0.5 m by 3 mm column packed with material sold under the name PORAPACKTM N.
• stage I reactor Process conditions for stage I reactor: 286°C/200 psi
• stage I reactor Process conditions for stage I reactor: 286°C/200 psi.
• the catalytic methods used show high selectivity to vinyl acetate by oxidizing mixtures of ethane and ethylene .

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
• Catalysts (AREA)

Priority Applications (5)

Applications Claiming Priority (2)

Publications (2)

Family

ID=23212532

Family Applications (1)

Country Status (10)

Cited By (8)

Families Citing this family (31)

Citations (3)

Family Cites Families (16)

• 1999
  • 1999-05-14 US US09/312,683 patent/US6143921A/en not_active Ceased
  • 1999-07-28 SA SA99200395A patent/SA99200395B1/ar unknown
• 2000
  • 2000-05-09 AT AT00936733T patent/ATE306467T1/de not_active IP Right Cessation
  • 2000-05-09 DE DE60023132T patent/DE60023132T2/de not_active Expired - Lifetime
  • 2000-05-09 US US10/031,808 patent/US6605739B1/en not_active Expired - Lifetime
  • 2000-05-09 ES ES00936733T patent/ES2250137T3/es not_active Expired - Lifetime
  • 2000-05-09 JP JP2000618222A patent/JP2002544250A/ja active Pending
  • 2000-05-09 WO PCT/EP2000/004234 patent/WO2000069802A1/en not_active Ceased
  • 2000-05-09 CN CNB008101868A patent/CN1188387C/zh not_active Expired - Fee Related
  • 2000-05-09 EP EP00936733A patent/EP1180092B1/en not_active Revoked
  • 2000-05-09 KR KR1020017014540A patent/KR100609203B1/ko not_active Expired - Fee Related
• 2006
  • 2006-02-08 US US11/363,148 patent/USRE43859E1/en not_active Expired - Lifetime

Patent Citations (3)

Also Published As

Similar Documents

Legal Events