WO2016144315A1 - Catalyst agglomeration remediation - Google Patents
Catalyst agglomeration remediation Download PDFInfo
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- WO2016144315A1 WO2016144315A1 PCT/US2015/019461 US2015019461W WO2016144315A1 WO 2016144315 A1 WO2016144315 A1 WO 2016144315A1 US 2015019461 W US2015019461 W US 2015019461W WO 2016144315 A1 WO2016144315 A1 WO 2016144315A1
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- WIPO (PCT)
- Prior art keywords
- reactor
- steam
- purge stream
- ethylbenzene
- catalyst
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- 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
- B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
- B01J8/02—Chemical 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
- B01J8/04—Chemical 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
- B01J8/0496—Heating or cooling the reactor
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- 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
- B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
- B01J8/02—Chemical 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
- B01J8/0207—Chemical 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 flow within the bed being predominantly horizontal
- B01J8/0221—Chemical 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 flow within the bed being predominantly horizontal in a cylindrical shaped bed
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- 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
- B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
- B01J8/02—Chemical 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
- B01J8/0278—Feeding reactive fluids
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- 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
- B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
- B01J8/02—Chemical 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
- B01J8/0285—Heating or cooling the reactor
-
- 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
- B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
- B01J8/02—Chemical 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
- B01J8/04—Chemical 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
- B01J8/0492—Feeding reactive fluids
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- 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
- B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
- B01J8/02—Chemical 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
- B01J8/06—Chemical 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
- B01J8/062—Chemical 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 being installed in a furnace
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/32—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
- C07C5/321—Catalytic processes
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/32—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
- C07C5/327—Formation of non-aromatic carbon-to-carbon double bonds only
- C07C5/333—Catalytic processes
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- 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
- B01J2208/00—Processes carried out in the presence of solid particles; Reactors therefor
- B01J2208/00008—Controlling the process
- B01J2208/00017—Controlling the temperature
- B01J2208/00327—Controlling the temperature by direct heat exchange
- B01J2208/00336—Controlling the temperature by direct heat exchange adding a temperature modifying medium to the reactants
- B01J2208/00353—Non-cryogenic fluids
- B01J2208/00371—Non-cryogenic fluids gaseous
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- 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
- B01J2208/00—Processes carried out in the presence of solid particles; Reactors therefor
- B01J2208/00008—Controlling the process
- B01J2208/00017—Controlling the temperature
- B01J2208/00504—Controlling the temperature by means of a burner
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- 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
- B01J2208/00—Processes carried out in the presence of solid particles; Reactors therefor
- B01J2208/00008—Controlling the process
- B01J2208/00628—Controlling the composition of the reactive mixture
- B01J2208/00637—Means for stopping or slowing down the reaction
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- 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
- B01J2208/00—Processes carried out in the presence of solid particles; Reactors therefor
- B01J2208/00008—Controlling the process
- B01J2208/00654—Controlling the process by measures relating to the particulate material
- B01J2208/00681—Agglomeration
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/02—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the alkali- or alkaline earth metals or beryllium
- C07C2523/04—Alkali metals
Definitions
- Embodiments of the present disclosure generally relate to catalyst agglomeration remediation.
- Polymers of styrene are common and valuable plastics that may be used in the production of items from electronics casing to toys to disposable plates and cups.
- the chemical formula of styrene monomer is C6H5C2H3, and its structure includes a benzene ring with an attached ethylene group.
- Styrene is generally produced by dehydrogenation of ethylbenzene.
- Ethylbenzene has the chemical formula of C6H5C2H5, and its structure includes a benzene ring with an attached ethyl group.
- Ethylbenzene dehydrogenation takes place in a dehydrogenation reactor system, which may include one or more dehydrogenation reaction chambers and downstream processing equipment.
- Superheated steam and ethylbenzene enter the reaction chamber(s) as an input steam where a dehydrogenation catalyst catalyzes the conversion of ethylbenzene to styrene.
- the mechanism for the dehydrogenation reaction involves the loss of two hydrogen atoms from the ethyl group to form a carbon-carbon double bond.
- the chemicals exiting the reaction chamber(s) generally include styrene, hydrogen gas, and steam, as well as unreacted ethylbenzene and other compounds, which may be referred to as styrene offgas.
- a shutdown procedure for a dehydrogenation reactor system includes cooling down the dehydrogenation reaction chambers under a steam-only purge.
- Catalyst agglomeration may increase the length of time that it takes to complete a turnaround.
- Catalyst agglomeration may include the formation clumped catalyst extrudite beds within the dehydrogenation reactor system, which may be fused with potassium.
- Catalyst agglomeration may be at least in-part caused by potassium migration and long run times of the dehydrogenation reactor system.
- potassium is a major catalyst component and may form KOH (potassium hydroxide) with steam at elevated temperatures.
- KOH has a significant vapor pressure and low melting point, allowing KOH to become mobile at reaction conditions.
- High potassium content and long run lengths with steam dilution may increase the severity of catalyst agglomeration in dehydrogenation reactor systems.
- An embodiment of the present disclosure includes a process.
- the process includes shutting down a reactor in which ethylbenzene is undergoing dehydrogenation to styrene in the presence of steam and a catalyst adapted to catalyze dehydrogenation of ethylbenzene to styrene.
- Shutting down the reactor includes reducing a temperature of the reactor, increasing a steam-to- ethylbenzene molar ratio of an input stream to the reactor to form a purge stream, and supplying the purge stream to the reactor.
- An embodiment of the present disclosure includes a process.
- the process includes shutting down a reactor in which ethylbenzene is undergoing dehydrogenation to styrene in the presence of a catalyst including potassium that is adapted to catalyze dehydrogenation of ethylbenzene to styrene.
- Shutting down the reactor includes reducing a temperature of the reactor, increasing a steam-to-ethylbenzene molar ratio of an input stream to the reactor to form a purge stream, and supplying the purge stream to the reactor.
- the process includes stopping supply of the purge stream to the reactor and supplying an inert gas purge stream to the reactor. Shutting down the reactor is performed without use of a steam-only purge stream.
- An embodiment of the present disclosure includes a process.
- the process includes shutting down a reactor in which ethylbenzene is undergoing dehydrogenation to styrene in the presence of a catalyst adapted to catalyze dehydrogenation of ethylbenzene to styrene.
- Shutting down the reactor includes reducing a temperature of the reactor and supplying a purge stream to the reactor.
- the purge stream includes steam and one or more of H2, CO2, and styrene.
- FIG. 1 depicts a plot of percent conversion of ethylbenzene versus reactor temperature for low temperature, high steam-to-oil ratios.
- FIG. 2 depicts a plot of average crush strength versus temperature for different catalyst shutdown procedures.
- Ethylbenzene dehydrogenation takes place in a dehydrogenation reactor system, which may include one or more dehydrogenation reaction chambers and downstream processing equipment.
- Superheated steam and ethylbenzene enter the reaction chamber(s) as an input stream where a catalyst catalyzes the conversion of ethylbenzene to styrene.
- the steam-to- ethylbenzene molar ratio during ethylbenzene dehydrogenation may be at least about 4: 1, at least about 5: 1, at least about 8: 1, or at least about 10: 1, for example.
- the ethylbenzene dehydrogenation reaction is generally run at a temperature of around 500°C to 650°C and atmospheric to sub-atmospheric pressure, such as around 5 to 20 psia.
- One or more embodiments relate to a process for shutting down a reactor in which ethylbenzene is undergoing dehydrogenation to styrene in the presence of a catalyst adapted to catalyze dehydrogenation of ethylbenzene to styrene.
- the steam-to-ethylbenzene molar ratio of purge stream may be greater than the steam-to-ethylbenzene molar ratio of the input stream, and supplying purge steam may include increasing the steam-to-ethylbenzene molar ratio of the input stream.
- Increasing the steam-to-ethylbenzene molar ratio may include increasing an amount of steam input into the reactor, decreasing an amount of ethylbenzene input into the reactor, or combinations thereof.
- the steam-to-ethylbenzene molar ratio of purge stream is maintained at from 12: 1 to 50: 1 while the temperature of the reactor is further reduced to a temperature ranging from less than 650°C to 360°C.
- the steam-to-ethylbenzene molar ratio of purge stream may be continuously maintained at from 12: 1 to 50: 1, or from 15: 1 to 40: 1, or from 20: 1 to 30: 1 while the temperature of the reactor is within the range of 550°C to 450°C during the shutting down of the reactor.
- Purge stream may include steam and one or more of H2, CO2, and styrene.
- one or more of H2, CO2, and styrene may be present as byproducts of dehydrogenation of ethylbenzene, or may be added to steam prior to introduction into the reactor.
- the input stream that includes steam and ethylbenzene may be supplied to the reactor.
- Supplying purge stream may include stopping supply of ethylbenzene to the reactor and adding one or more of H2, CO2, and styrene with the steam.
- the presence of steam and one or more of H2, CO2, and styrene in purge stream may be maintained while the temperature of the reactor is further reduced to a temperature ranging from less than 650°C to 360°C.
- the presence of steam and one or more of H2, CO2, and styrene in purge stream may be continuously maintained while the temperature of the reactor is within the range of 550°C to 450°C during the shutting down of the reactor.
- the supplying of purge stream may begin after the temperature of the reactor is reduced, while the temperature of the reactor is being reduced, or before the temperature of the reactor is reduced.
- a steam-only purge stream may be a purge stream that includes steam but does not include one or more of ethylbenzene, H2, CO2, and styrene.
- a steam-only purge stream may be a purge steam that only includes steam. In certain embodiments, shutting down the reactor is performed without use of a steam-only purge stream at conditions where potassium agglomeration is most problematic.
- the process may include stopping supply of purge stream to the reactor and supplying an inert gas purge stream to the reactor.
- Inert gas purge stream may include nitrogen, for example.
- the process may include further reducing the temperature of the reactor.
- the temperature of the reactor may be further reduced to a temperature ranging from 20°C to 400°C, or to a temperature of at most 400°C, or at most 360°C, or at most 300°C.
- the temperature in the reactor may be held constant while supplying inert gas purge stream to the reactor for a period of time ranging from 1 to 24 hours, or from 4 to 18 hours, or from 6 to 16 hours, or from 8 to 14 hours, or from 10 to 12 hours.
- the temperature may be held constant prior to a further reduction in the temperature.
- the catalyst or agglomerated masses of catalyst particles may exhibit an average crush strength that is lower than an average crush strength exhibited by the catalyst prior to shutting down the reactor.
- the catalyst may exhibit an average crush strength that is at least 10%, or at least 15%, or at least 25%, or at least 40% or at least 50% lower than an average crush strength exhibited by the catalyst prior to shutting down the reactor.
- Average crush strength may be measured in accordance with ASTM D4179-11.
- Tube Furnace Experiments. Initial exploratory experiments were conducted with a 30" long, horizontal tube furnace and a 1" internal diameter (ID) metal tube reactor with steam injection. Used catalyst samples were wrapped in wire mesh and held in place axially with a metal rod. Water was fed to the unit at 0.5 mL/min at temperatures ranging from 350°C to 550°C. The reactor was purged with nitrogen at temperature before unloading to keep the samples dry. The used catalyst samples were heated at various temperatures in steam to identify K migration leading to catalyst agglomeration. Particles of used catalyst, when mixed with potassium carbonate, were observed to be cemented together after treatment to qualitatively demonstrate agglomeration. Significant variation in the repeat experiments was caused by inconsistent particle to particle contact; however, both K migration and catalyst agglomeration were clearly demonstrated in the lab.
- ID internal diameter
- a typical shutdown procedure generally involves initially removing the flow of ethylbenzene, and subsequently replacing the flow of steam with nitrogen as the catalyst bed cools.
- steam and ethylbenzene flow across the catalyst bed as the reactor temperatures are lowered.
- the ethylbenzene flow is generally stopped. The temperature at which the flow of ethylbenzene is stopped may vary depending upon the catalyst used.
- the typical shutdown procedure will generally then include cooling under a steam-only flow until a temperature of about 425°C (797 °F) is reached, and then the steam will be replaced by a circulating nitrogen purge.
- the period of cooling under the steam-only flow may cause strengthening of the catalyst agglomeration as the melting point of KOH is 360°C (680°F).
- a lab test was developed to study catalyst agglomeration using composite pellets prepared from used catalyst powders and potassium carbonate. The pellets were placed in a reactor and subjected to various conditions followed by crush strength testing of the experimental pellets. A high steam-to-ethylbenzene molar ratio sequence lessened catalyst agglomeration versus steam-only conditions at elevated temperatures.
- Test pellets were prepared from used catalyst powder and potassium carbonate. The powders were screened with a 14 mesh sieve and mixed in a 70:30 weight ratio of used catalysts to potassium carbonate. The mixture was pressed with a plunger die set at 2000 psi into a 13 mm diameter pellet using 1.5 g of powder mixture for each pellet. The pellet thickness was about 6.5 mm. The pellets (4 per experiment) were secured in a screen wire basket attached to the end of a supporting metal rod. A 1" reactor without an internal thermal well was used to test the 13 mm used catalyst/potassium carbonate pellets.
- This pellet preparation method was designed to simulate the state of catalyst in the reactors at the end of a run where there are external deposits of potassium mixed with used catalyst under the weight of a fully loaded reactor. Runs were also made with a 2" bed of used catalyst upstream from the test pellets in order to simulate a reaction stream with dehydrogenation products. Experiments 1-4, as detailed below, were conducted to simulate several different scenarios.
- Experiment 1 Increases in crush strength correlate with increasing catalyst agglomeration. Decreases in crush strength correlates with decreasing catalyst agglomeration.
- Experiment 1 was conducted to determine the status of the catalyst during the run by quenching the catalyst pellets with rapid cooling and a high flow of nitrogen. Experiment 1 serves as a reference point before initiating a shutdown procedure. In Experiment 2 the catalyst was subjected to a slow cool down with a nitrogen purge. A pellet strengthening was observed, that is the crush strength of the catalyst pellets was increased relative to Experiment 1.
- Experiment 3 most closely resembles a typical shutdown procedure under steam. Experiment 3 showed an increase in pellet crush strength.
- Experiment 4 evaluated a high steam-to-ethylbenzene molar ratio. The catalyst pellets in Experiment 4 exhibited a decrease in crush strength relative to Experiment 1. The catalyst pellets in Experiment 4 were noticeably weaker when handled.
- Example 4 expanded upon the temperature range of the experiments in Example 3, and investigated the hydrogen effect with steam.
- the experiments of Example 4 used test pellets made from compressed used catalyst powder and potassium carbonate, as in Example 3. The pellets were loaded in the isothermal reactor downstream from a small catalyst bed and conditioned at typical run conditions.
- Test pellets were prepared from used catalyst powder of a promoted potassium and iron oxide industrial formulation and potassium carbonate. The powders were screened with a 14 mesh sieve and mixed in a 70:30 weight ratio of used catalysts to potassium carbonate. The mixture was pressed with a plunger die set at 2000 psi into a 13 mm diameter pellet using 1.5 g of powder mixture for each pellet. The pellet thickness was about 6.5 mm. The pellets were secured in a screen wire basket attached to the end of a supporting metal rod. A 1" reactor without an internal thermal well was used to test the 13 mm used catalyst/potassium carbonate pellets.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- Fluid Mechanics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
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Abstract
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Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201580077616.1A CN107406343B (en) | 2015-03-09 | 2015-03-09 | Catalyst agglomeration remediation |
KR1020177027680A KR102349195B1 (en) | 2015-03-09 | 2015-03-09 | Improved catalyst agglomeration |
JP2017547518A JP6701226B2 (en) | 2015-03-09 | 2015-03-09 | Catalyst aggregation improvement |
EP15884843.2A EP3268338B1 (en) | 2015-03-09 | 2015-03-09 | Catalyst agglomeration remediation |
BR112017018980-1A BR112017018980B1 (en) | 2015-03-09 | 2015-03-09 | PROCESSES FOR STYLENE PRODUCTION IN THE PRESENCE OF STEAM AND A CATALYST ADAPTED TO CATALYST THE DEHYDROGENATION OF ETHYLBENZENE IN STYLENE |
CA2978867A CA2978867C (en) | 2015-03-09 | 2015-03-09 | Catalyst agglomeration remediation |
EA201700421A EA036034B1 (en) | 2015-03-09 | 2015-03-09 | Catalyst agglomeration remediation |
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Application Number | Priority Date | Filing Date | Title |
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US14/642,204 | 2015-03-09 | ||
US14/642,204 US9623392B2 (en) | 2015-03-09 | 2015-03-09 | Catalyst agglomeration remediation |
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WO2016144315A1 true WO2016144315A1 (en) | 2016-09-15 |
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PCT/US2015/019461 WO2016144315A1 (en) | 2015-03-09 | 2015-03-09 | Catalyst agglomeration remediation |
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US (1) | US9623392B2 (en) |
EP (1) | EP3268338B1 (en) |
JP (1) | JP6701226B2 (en) |
KR (1) | KR102349195B1 (en) |
CN (1) | CN107406343B (en) |
BR (1) | BR112017018980B1 (en) |
CA (1) | CA2978867C (en) |
EA (1) | EA036034B1 (en) |
TW (1) | TWI723971B (en) |
WO (1) | WO2016144315A1 (en) |
Citations (6)
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US4347396A (en) * | 1980-03-27 | 1982-08-31 | Mitsubishi Petrochemical Co., Ltd. | Process for producing styrene |
US5258348A (en) * | 1989-10-31 | 1993-11-02 | The Dow Chemical Company | Supported catalyst for the dehydrogenation of hydrocarbons and method for the preparation of the catalyst |
US5461179A (en) * | 1993-07-07 | 1995-10-24 | Raytheon Engineers & Constructors, Inc. | Regeneration and stabilization of dehydrogenation catalysts |
WO2001044146A1 (en) * | 1999-12-17 | 2001-06-21 | Dow Global Technologies Inc. | Dehydrogenation of an alkyl aromatic compound and catalyst regeneration in a fluidized bed reactor |
US20050080306A1 (en) | 2003-10-14 | 2005-04-14 | Kowaleski Ruth Mary | Method of operating a dehydrogenation reactor system |
US20090318743A1 (en) * | 2008-06-19 | 2009-12-24 | Arnold Stephen C | Combined carbon dioxide and oxygen process for ethylbenzene dehydrogenation to styrene |
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JPH04134038A (en) * | 1990-09-25 | 1992-05-07 | Asahi Chem Ind Co Ltd | Production of alkenylbenzene |
US20090318741A1 (en) * | 2008-04-09 | 2009-12-24 | Newman Richard Douglas | Method of improving a dehydrogenation process |
US20100081855A1 (en) * | 2008-09-30 | 2010-04-01 | Fina Technology, Inc. | Semi-Supported Dehydrogenation Catalyst |
CN101992129B (en) * | 2009-08-31 | 2013-03-06 | 中国石油化工股份有限公司 | Potassium supplementing method of styrene catalyst prepared via ethyl benzene dehydrogenation |
JP6446427B2 (en) * | 2013-03-14 | 2018-12-26 | クラリアント コーポレイション | How to stop the reactor |
-
2015
- 2015-03-09 WO PCT/US2015/019461 patent/WO2016144315A1/en active Application Filing
- 2015-03-09 EA EA201700421A patent/EA036034B1/en not_active IP Right Cessation
- 2015-03-09 CA CA2978867A patent/CA2978867C/en not_active Expired - Fee Related
- 2015-03-09 BR BR112017018980-1A patent/BR112017018980B1/en not_active IP Right Cessation
- 2015-03-09 US US14/642,204 patent/US9623392B2/en active Active
- 2015-03-09 CN CN201580077616.1A patent/CN107406343B/en active Active
- 2015-03-09 KR KR1020177027680A patent/KR102349195B1/en active IP Right Grant
- 2015-03-09 JP JP2017547518A patent/JP6701226B2/en not_active Expired - Fee Related
- 2015-03-09 EP EP15884843.2A patent/EP3268338B1/en active Active
- 2015-12-24 TW TW104143628A patent/TWI723971B/en not_active IP Right Cessation
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4347396A (en) * | 1980-03-27 | 1982-08-31 | Mitsubishi Petrochemical Co., Ltd. | Process for producing styrene |
US5258348A (en) * | 1989-10-31 | 1993-11-02 | The Dow Chemical Company | Supported catalyst for the dehydrogenation of hydrocarbons and method for the preparation of the catalyst |
US5461179A (en) * | 1993-07-07 | 1995-10-24 | Raytheon Engineers & Constructors, Inc. | Regeneration and stabilization of dehydrogenation catalysts |
WO2001044146A1 (en) * | 1999-12-17 | 2001-06-21 | Dow Global Technologies Inc. | Dehydrogenation of an alkyl aromatic compound and catalyst regeneration in a fluidized bed reactor |
US20050080306A1 (en) | 2003-10-14 | 2005-04-14 | Kowaleski Ruth Mary | Method of operating a dehydrogenation reactor system |
US20090318743A1 (en) * | 2008-06-19 | 2009-12-24 | Arnold Stephen C | Combined carbon dioxide and oxygen process for ethylbenzene dehydrogenation to styrene |
Non-Patent Citations (2)
Title |
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DR. ARNO BEHR, STYRENE PRODUCTION FROM ETHYLBENZENE, Retrieved from the Internet <URL:http://www.tc.bci.tu-dortmund.de/Downloads/Praktika/tc30styreneenalish.pdf> |
See also references of EP3268338A4 |
Also Published As
Publication number | Publication date |
---|---|
EP3268338A1 (en) | 2018-01-17 |
US9623392B2 (en) | 2017-04-18 |
CN107406343A (en) | 2017-11-28 |
EP3268338A4 (en) | 2018-10-24 |
JP2018509414A (en) | 2018-04-05 |
BR112017018980A2 (en) | 2018-05-22 |
TW201638057A (en) | 2016-11-01 |
US20160263543A1 (en) | 2016-09-15 |
EA036034B1 (en) | 2020-09-16 |
EA201700421A1 (en) | 2018-02-28 |
KR102349195B1 (en) | 2022-01-10 |
EP3268338B1 (en) | 2021-01-06 |
JP6701226B2 (en) | 2020-05-27 |
CA2978867C (en) | 2020-10-13 |
TWI723971B (en) | 2021-04-11 |
KR20170127491A (en) | 2017-11-21 |
BR112017018980B1 (en) | 2020-10-06 |
CN107406343B (en) | 2021-10-26 |
CA2978867A1 (en) | 2016-09-15 |
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