EP1660225A1 - Oxidationsverfahren und reaktor mit modifierter zurührvorrichtung - Google Patents

Oxidationsverfahren und reaktor mit modifierter zurührvorrichtung

Info

Publication number
EP1660225A1
EP1660225A1 EP03818197A EP03818197A EP1660225A1 EP 1660225 A1 EP1660225 A1 EP 1660225A1 EP 03818197 A EP03818197 A EP 03818197A EP 03818197 A EP03818197 A EP 03818197A EP 1660225 A1 EP1660225 A1 EP 1660225A1
Authority
EP
European Patent Office
Prior art keywords
reactor
feed
short bed
gas mixture
plenum
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Withdrawn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
EP03818197A
Other languages
English (en)
French (fr)
Inventor
Olan Stanley Fruchey
Brian Robert Keyes
Carl David Murphy
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.)
Dow Global Technologies LLC
Original Assignee
Dow Global Technologies LLC
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
Application filed by Dow Global Technologies LLC filed Critical Dow Global Technologies LLC
Publication of EP1660225A1 publication Critical patent/EP1660225A1/de
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/16Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
    • C07C51/21Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
    • C07C51/215Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of saturated hydrocarbyl groups
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/008Details of the reactor or of the particulate material; Processes to increase or to retard the rate of reaction
    • B01J8/0085Details of the reactor or of the particulate material; Processes to increase or to retard the rate of reaction promoting uninterrupted fluid flow, e.g. by filtering out particles in front of the catalyst layer
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/02Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds
    • B01J8/0278Feeding reactive fluids
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/02Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds
    • B01J8/04Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds the fluid passing successively through two or more beds
    • B01J8/0446Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds the fluid passing successively through two or more beds the flow within the beds being predominantly vertical
    • B01J8/0476Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds the fluid passing successively through two or more beds the flow within the beds being predominantly vertical in two or more otherwise shaped beds
    • B01J8/048Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds the fluid passing successively through two or more beds the flow within the beds being predominantly vertical in two or more otherwise shaped beds the beds being superimposed one above the other
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/02Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds
    • B01J8/06Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds in tube reactors; the solid particles being arranged in tubes
    • B01J8/067Heating or cooling the reactor
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/16Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
    • C07C51/21Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
    • C07C51/25Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring
    • C07C51/252Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring of propene, butenes, acrolein or methacrolein
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/00008Controlling the process
    • B01J2208/00017Controlling the temperature
    • B01J2208/00106Controlling the temperature by indirect heat exchange
    • B01J2208/00168Controlling the temperature by indirect heat exchange with heat exchange elements outside the bed of solid particles
    • B01J2208/00212Plates; Jackets; Cylinders
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/00008Controlling the process
    • B01J2208/00017Controlling the temperature
    • B01J2208/00522Controlling the temperature using inert heat absorbing solids outside the bed
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/30Details relating to random packing elements
    • B01J2219/304Composition or microstructure of the elements
    • B01J2219/30416Ceramic

Definitions

  • TECHNICAL FIELD This invention relates to improvements for processes using shell and tube reactors. More specifically, the invention relates to using a short bed of packing material to direct leakage of contaminants such as heat exchange media or derivatives thereof away from the headspace of a tubular reactor and prevent formation of combustible gas mixtures.
  • BACKGROUND Tubular reactors are often times used for exothermic reactions, for example, the oxidation of propylene to acrylic acid and the manufacture of maleic anhydride.
  • production of acrylic acid is a two-stage gaseous catalytic oxidation of propylene.
  • the method employs a first stage reactor with a first stage catalyst for oxidation of propylene to acrolein and a second stage reactor charged with a second stage catalyst suitable for oxidation of acrolein to acrylic acid.
  • admixed feed reactants for example, propylene, air and steam used to produce acrylic acid are not expected to ignite at temperatures lower than about 450°C.
  • 5,080,872 discloses a method of regulating temperature inside a reaction vessel using a bed of solid particles having varied temperature zones through which a reactant fluid phase is passed.
  • United States Patent No. 6,028,220 discloses to the oxidation of propylene during which there is a reduction of hot spots in the catalyst layer by varying the catalyst activity; whereas, United States Patent No. 6,563,000 describes a process of producing acrylic acid from acrolein that includes multiple reaction zones wherein each such reaction zone comprises a catalyst of a different activity level, as compared to an adjacent zone, as is well known. Controlling temperature by circulating particulate matter, in general, has been disclosed, see, for example, United States Patent No.
  • United States Patent No. 4,672,918 discloses circulating temperature controlled solids to control the temperature of a fluidized bed.
  • United States Patent No. 4,899,695 discloses a process for controlling heat transfer and erosion in a fluidized bed combustion reactor by introducing particles into the combustion unit along with or in the presence of combustion reactants whereby some of the particles may be recycled.
  • United States Patent No. 5,505,907 describing a method for controlling the temperature of an incoming gas stream by incorporating coated solid particles into the gas stream, circulating and separating such particles and thereafter recycling same for repeat use.
  • 4,029,636 which discloses a method for removing molybdenum trioxide from reactor effluent gases issuing from reactors containing molybdenum-based catalysts by causing the effluent gases to pass over a bed of cooled solids located at the exit end of the tubular reactor on which the molybdenum trioxide is deposited.
  • United States Patent No. 5,413,699 discloses removal of NO x by forcing NO x containing gas through a DeNO catalyst bed.
  • 5,538,544 discloses a pressure swing adsorption system whereby a gas is introduced into the vessel head of such a pressure swing system and caused to distribute uniformly on an adsorbent bed as a result of passing through a graded ball bed support system.
  • the methods described above for controlling contamination require somewhat specialized environments and/or construction and use, and accordingly, they are simply not practical for retrofitting existing equipment to limit contamination in the event of a reactor breach, for example, where heat exchange fluid may leak and form derivatives and mix with the reactor feed.
  • the invention is based, in part, on the discovery that a short bed of packing material in the vicinity of the inlets of reactor tubes of a shell and tube reactor can restrict migration of decomposition gases (i.e., NOx) from heat exchange media into the reactor headspace. It has been found that such a bed placement virtually eliminates auto-ignition problems stemming from heat-exchange media leaks. It has been found that a short bed suffices to ameliorate contaminant problems without the need for a deeper bed and its associated pressure drop and material expense.
  • decomposition gases i.e., NOx
  • the invention relates to an improved process for high temperature oxidation of a gaseous reactant in a shell and tube reactor of the class with a plurality of reactor tubes wherein the reactor tubes are immersed in a heat exchange medium contained within the shell and the interior volume of the reactor tubes is thereby isolated from the heat exchange medium.
  • the reactor tube interior inlets are in communication with a feed plenum or headspace having a characteristic cross-sectional area in the vicinity of the reactor tube inlets generally free from obstruction, such that the velocity of a feed gas mixture to the reactor tube inlets is the volume rate of flow of the feed gas mixture divided by the characteristic cross-sectional area of the plenum in the vicinity of the reactor tube inlets.
  • the process is also of the class wherein the feed gas mixture is fed from the plenum to the reactor tubes.
  • the improvement of the present invention includes disposing a short bed of packing material adjacent to the reactor tube inlets.
  • the short bed can include a voidage of from about 0.3 to about 0.75 to increase the velocity of the feed gas mixture in the vicinity of the reactor tube inlets whereby contamination of the feed plenum by the decomposition gases of the heat exchange medium is controlled in the event of a reactor breach in the vicinity of the reactor tube inlets, as might occur when heat exchange medium leaks between the tubes and end plate due to corrosion.
  • the short bed occupies less than 20 percent of the headspace volume and preferably less than about 10 percent of the headspace volume.
  • the packing material comprises spherical macroparticles having diameters from about 0.125 to about 4 inches. Most preferred are ceramic macroparticles having a diameter of less than about 2 inches.
  • Alternate packing material shapes may be selected from pellets, disks, rods and plates of various shapes. DENSTONE® balls, available from Norton (Akron, OH, USA) are particularly preferred.
  • the inventive process and apparatus may be used in connection with the manufacture of methacrylic acid, maleic anhydride, acrylic acid and potentially other partial oxidations as may occur in the manufacture of ethylene oxide or vinyl acetate monomer, for example.
  • an improvement to a shell and tube reactor having tubes immersed in a heat-exchange medium at a temperature of 200-400°C which includes adding a short bed of packing material about the reactor tube inlets as described below.
  • the short bed has a depth of from about 10 to about 25 inches, while the reactor tubes have an inside diameter of about 0.75 to about 2 inches in preferred embodiments.
  • the improved reactor is suitably employed in the manufacture of acrylic acid as described below. Controlling contaminants, for example, oxidizers such as nitrogen oxides, can control flammability and undesired spontaneous auto-ignition. Adequate flow velocity prevents temperature excursions when the feed gas mixture and contaminants combine to form a mixture of increased flammability.
  • the bed placement could prevent undesirable migration of contaminants to the headspace whether or not contaminants increase flammability.
  • a contaminant could be a catalyst poison, thus, the contaminant needs to be restricted to localized regions of the reactor rather than be ubiquitous in the headspace so that it is fed to all of the tubes.
  • FIGURE 1 is a schematic diagram illustrating the process and apparatus of the present invention.
  • FIGURE 2 is a graph illustrating the spontaneous ignition of feed gas stream in the presence of 0.2% NO.
  • Like reference symbols in the various drawings indicate like elements.
  • Nitrogen oxides can include nitric oxide (NO), nitrous oxide (N 2 O), and nitrogen dioxide (NO ) among others. Presence of nitrogen oxides in low levels, for example, 10 to 9000 ppm can act as an oxidizer and lower ignition temperature of the feed gas mixture as may occur when the heat exchange medium leaks into the headspace. For example, a feed gas mixture of 7% propylene / 60% air / 30% steam is stable at a temperature of about 450°C.
  • Presence of 5000 ppm of nitrogen oxides can lower the ignition temperature to, for example, 300°C.
  • Presence of a short bed of packing material adjacent to the reactor tube inlets may prevent migration of contaminants into the headspace, or quench autoignition in the presence of nitrogen oxides or decrease residence time of combustible mixture in the reactor or confine the contaminants to the area where the leakage occurred or alternatively, alter the temperature profile of the reactor. Regardless of theory, the short bed has been found remarkably effective in ameliorating autoignition problems.
  • "macroparticle” is any solid three-dimensional object having a volume of at least about 0.015 ml or more; preferably more than about 0.1 ml or more.
  • FIGURE 1 shows a shell and tube reactor 10, which includes a head 15 defining a feed plenum or headspace 20, a short bed of packing material 30, a heat exchanger shell 40 and a plurality of reactor tubes 50 disposed in the reactor.
  • the feed plenum includes a distributor 60 for admixing reactants in a feed gas mixture.
  • the feed plenum 20 is in communication with the plurality of reactor tubes 50 in a heat exchanger 40, through an end plate 55.
  • the dimensions of the feed plenum or headspace 20 can vary with the cross-section area of the reactor tubes in the reactor 10.
  • the feed plenum can be from about 5 to about 14 feet tall, with a diameter of the feed plenum from about 2 to about 20 feet.
  • the plurality of reactor tubes 50 with reactor tube inlets 70 are surrounded by a heat exchanger medium 80.
  • the heat exchange medium 80 can be a salt.
  • the salt coolant can include melts of salts. Suitable salts include potassium nitrate, potassium nitrite, sodium nitrite and/or sodium nitrate or metals having a low melting point, for example, sodium, mercury or alloys of various metals.
  • the temperature of the heat exchange medium can be less than 450°C, more preferably about 420°C.
  • Dupont's HITEC salt can be used, which includes about 53% potassium nitrate, about 40% sodium nitrate, and about 7% sodium nitrate.
  • Contaminants formed by decomposition of anions in salt coolant can leak through the end plate area 65 into the feed plenum 20 in the event of a reactor break. It is believed that the salt leaks first and then decomposes in the presence of rust and oxidation catalyst.
  • the short bed of packed material 30 is disposed adjacent to the reactor tube inlets 70, extending horizontally in the plenum.
  • the short bed 30 includes discrete inert macroparticles of, for example, ceramic material.
  • the short bed of packing material 30 can vary in dimensions. Suitable depth, H, of the short bed can be less than 24 inches or so but at least 5 inches; typically, 1 foot or so. Shape of such inert macroparticles is not critical.
  • the macroparticles may be granular, such as a sphere, pellet, disk, hollow tube, spherical, cylindrical, ring-formed, or may be in the forms of rods, plates, and wire net or in the form of aggregates thereof.
  • Suitable macroparticles can be spheres. When granular or other inert substances are used, their sizes are not necessarily uniform.
  • the diameter of the sphere can be from about 1/16 inch to about 2 inches, preferably about 0.25 inch diameter.
  • the size of the macroparticles is most preferably not larger than the diameter of reactor tubes (ca. 1") in the reactor, so as to not occlude the reactor tubes.
  • the short bed 30 has a substantial voidage so as not to cause too much of a pressure drop or pressure differential during the passage of feed gas mixture to the reactor tubes.
  • the voidage of the macroparticles in the short bed 30 can be from about 0.25 to about 0.75, preferably from about 0.3 to 0.5 and most preferably 0.4.
  • the packing density of the macroparticles can be from about 70 lbs/ft 3 to about 110 lbs/ft 3 , with from about 80-90 lbs/ft 3 being somewhat typical.
  • the spheres can be, for example, DENSTONE® spheres, which are commercially available for Norton Chemicals (Akron, OH, USA).
  • the DENSTONE® spheres can be, for example, DENSTONE®57, DENSTONE® 2000 or DENSTONE® 99.
  • the macroparticles can be ceramic, alumina, silica or clay in composition.
  • the short bed of packed material 30 provides an increase in velocity of the feed gas mixture to the reactor tube inlets because the cross section available for flow is decreased by the area occupied by the macroparticles.
  • Such an increase in velocity of the feed gas mixture sweeps contaminants such as oxidizers, for example, nitrogen oxides, stemming from end plate breaches into the reactor tubes 50 before they migrate into the plenum generally.
  • Adequate flow velocity and a streamlined flow path can reduce flammability in the feed plenum 20, where the feed gas mixture and contaminants can mix to cause a potential spontaneous ignition of the feed gas mixture.
  • Spontaneous auto-ignition can be controlled by passing the feed gas mixture to the reactor tubes in a time that is less than the time required for auto-ignition.
  • a method for producing acrylic acid from propylene in a two-stage catalytic oxidation using shell-and-tube heat exchanger type reactor have been described. See, for example, United States Patent Nos.
  • the distributor 60 conveys a feed gas mixture of reactants into the feed plenum or headspace 20.
  • the feed gas mixture expands into and through the feed plenum 20 to the short bed ⁇ f packed material 30.
  • the superficial velocity of the feed gas mixture into the feed plenum can be in the range of 3 to 10 ft/sec.
  • the feed gas mixture can include 7% propylene / 60% air / 30%> steam.
  • the feed gas mixture enters the short bed of packed material 30 adjacent to the reactor tubes inlets 70 of the reactor.
  • Optimum packing material can be determined by the size of the tubular reactor, gas flow combination, flow through the inlet plenum, desired pressure drop and velocity profile in the short bed.
  • a feed gas mixture including n-butane, and air passes via distributor 60 to feed plenum 20.
  • the feed gas mixture is distributed uniformly over the short bed of packing material 30 and passes to the reactor tubes 50.
  • n-butane reacts with oxygen in the air to produce maleic anhydride.
  • a feed gas mixture including isobutylene, and air passes via distributor 60 to feed plenum 20.
  • the feed gas mixture is distributed uniformly over the short bed of packing material 30 and passes to the reactor tubes 50.
  • isobutylene reacts with oxygen in the air to produce methacrylic acid.
  • Still other products, such as vinyl acetate or ethylene oxide may be made in accordance with the present invention.
  • COMPARATIVE EXAMPLE In a process for oxidation of propylene to acrylic acid, a tubular reactor including a plurality of reactor tubes having a cross-sectional area of (ca. 60 ft 2 open tube area; ca.
  • EXAMPLE 1 The reactor of the comparative example above was charged with a short bed of packing material of DENSTONE® l A" spheres. The depth of the short bed of packing material was 1 ft.
  • the reactor conditions were selected such that a temperature of ca. 620°F; 326°C and a pressure of ca. 16 psig; 1.1 bar gauge prevailed in the reactor with a composition of the feed gas mixture being ca. 7% propylene, ca. 60% air and ca. 30% steam.
  • the system was operated such that a circulating volume gas flow of ca. 1200 MSCFH was obtained. Autoignition of the feed was virtually eliminated by placement of the short bed about the reactor tube inlets, while yields and conversions were unchanged.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Physics & Mathematics (AREA)
  • Fluid Mechanics (AREA)
  • Devices And Processes Conducted In The Presence Of Fluids And Solid Particles (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Furan Compounds (AREA)
EP03818197A 2003-07-31 2003-07-31 Oxidationsverfahren und reaktor mit modifierter zurührvorrichtung Withdrawn EP1660225A1 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/US2003/023933 WO2005016509A1 (en) 2003-07-31 2003-07-31 Oxidation process and reactor with modified feed system

Publications (1)

Publication Number Publication Date
EP1660225A1 true EP1660225A1 (de) 2006-05-31

Family

ID=34192532

Family Applications (1)

Application Number Title Priority Date Filing Date
EP03818197A Withdrawn EP1660225A1 (de) 2003-07-31 2003-07-31 Oxidationsverfahren und reaktor mit modifierter zurührvorrichtung

Country Status (6)

Country Link
EP (1) EP1660225A1 (de)
JP (1) JP2007521126A (de)
CN (1) CN1819869A (de)
BR (1) BR0318401A (de)
MX (1) MXPA06001255A (de)
WO (1) WO2005016509A1 (de)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102004052331A1 (de) * 2004-10-27 2006-05-04 Nec Europe Ltd. Verfahren zur Steuerung der Kommunikation mit mobilen Stationen in einem Netzwerk
TWI390145B (zh) * 2008-03-31 2013-03-21 Rohm & Haas 用於爆燃壓力衰減之方法及設備
EP2485832B1 (de) 2009-10-09 2016-11-23 Blue Cube IP LLC Verfahren zur herstellung eines chlorierten und/oder fluorierten propens in einem isothermischen multiröhrenreaktoren
JP5767231B2 (ja) 2009-10-09 2015-08-19 ダウ グローバル テクノロジーズ エルエルシー 塩素化及び/又はフッ素化されたプロペン及びより高級なアルケンを製造するプロセス
EP2714631B1 (de) 2011-05-31 2020-05-13 Blue Cube IP LLC Verfahren zur herstellung von chlorierten propenen
US9233896B2 (en) 2011-08-07 2016-01-12 Blue Cube Ip Llc Process for the production of chlorinated propenes
US8907148B2 (en) 2011-08-07 2014-12-09 Dow Global Technologies Llc Process for the production of chlorinated propenes
WO2013078035A1 (en) 2011-11-21 2013-05-30 Dow Global Technologies, Llc Process for the production of chlorinated alkanes
CN104024187B (zh) 2011-12-02 2017-04-12 蓝立方知识产权有限责任公司 生产氯化烷烃的方法
CN104024186B (zh) 2011-12-02 2016-10-12 蓝立方知识产权有限责任公司 生产氯化烷烃的方法
JP6170068B2 (ja) 2011-12-13 2017-07-26 ブルー キューブ アイピー エルエルシー 塩素化プロパン及びプロペンの製造方法
EP2794528B1 (de) 2011-12-22 2020-02-26 Blue Cube IP LLC Verfahren zur herstellung von tetrachlormethan
BR112014015123A2 (pt) 2011-12-23 2017-06-13 Dow Global Technologies Llc processo para a produção de um ou mais alcenos ou compostos aromáticos
WO2014046970A1 (en) 2012-09-20 2014-03-27 Dow Global Technologies, Llc Process for the production of chlorinated propenes
CN104755448A (zh) 2012-09-20 2015-07-01 陶氏环球技术有限公司 用于制造氯化丙烯的方法
CN102861538A (zh) * 2012-09-28 2013-01-09 神华集团有限责任公司 列管式固定床反应器
EP2900364B1 (de) 2012-09-30 2018-06-13 Blue Cube IP LLC Wehrlöschung und verfahren damit
IN2015DN03949A (de) 2012-10-26 2015-10-02 Dow Global Technologies Llc
US9512053B2 (en) 2012-12-18 2016-12-06 Blue Cube Ip Llc Process for the production of chlorinated propenes
WO2014100039A1 (en) 2012-12-19 2014-06-26 Dow Global Technologies, Llc Process for the production of chlorinated propenes
JP2016507590A (ja) 2013-02-27 2016-03-10 ブルー キューブ アイピー エルエルシー 塩素化プロペンを生成するための方法
WO2014164368A1 (en) 2013-03-09 2014-10-09 Dow Global Technologies Llc Process for the production of chlorinated alkanes

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1066707C (zh) * 1994-04-05 2001-06-06 株式会社日本触媒 生产1,2,4,5-苯四酸酐的方法
US6013834A (en) * 1999-03-04 2000-01-11 Celanese International Corporation Production of vinyl acetate in a catalytic reactor equipped with filter and distribution bed
US6620968B1 (en) * 1999-11-23 2003-09-16 Rohm And Haas Company High hydrocarbon space velocity process for preparing unsaturated aldehydes and acids
DE10047693A1 (de) * 2000-09-25 2002-04-11 Basf Ag Verfahren zur Verlängerung der Standzeit von Katalysatoren

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
GEIRINGER P.L.: "Handbook of Heat Transfer Media", 1962, REINHOLD PUBLISHING CORPORATION, NEW YORK *
See also references of WO2005016509A1 *

Also Published As

Publication number Publication date
MXPA06001255A (es) 2006-05-15
CN1819869A (zh) 2006-08-16
BR0318401A (pt) 2006-08-01
JP2007521126A (ja) 2007-08-02
WO2005016509A1 (en) 2005-02-24

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