WO2020005781A1 - Processes and apparatuses for toluene and benzene methylation in an aromatics complex - Google Patents
Processes and apparatuses for toluene and benzene methylation in an aromatics complex Download PDFInfo
- Publication number
- WO2020005781A1 WO2020005781A1 PCT/US2019/038613 US2019038613W WO2020005781A1 WO 2020005781 A1 WO2020005781 A1 WO 2020005781A1 US 2019038613 W US2019038613 W US 2019038613W WO 2020005781 A1 WO2020005781 A1 WO 2020005781A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- reactor
- aromatic
- refractory
- paragraph
- toluene
- 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.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/86—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation between a hydrocarbon and a non-hydrocarbon
- C07C2/862—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation between a hydrocarbon and a non-hydrocarbon the non-hydrocarbon contains only oxygen as hetero-atoms
- C07C2/864—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation between a hydrocarbon and a non-hydrocarbon the non-hydrocarbon contains only oxygen as hetero-atoms the non-hydrocarbon is an alcohol
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/54—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition of unsaturated hydrocarbons to saturated hydrocarbons or to hydrocarbons containing a six-membered aromatic ring with no unsaturation outside the aromatic ring
- C07C2/64—Addition to a carbon atom of a six-membered aromatic ring
-
- 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
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/0006—Controlling or regulating processes
- B01J19/0013—Controlling the temperature of the process
-
- 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
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/0053—Details of 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
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/02—Apparatus characterised by being constructed of material selected for its chemically-resistant properties
-
- 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
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00049—Controlling or regulating processes
- B01J2219/00051—Controlling the temperature
-
- 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
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00049—Controlling or regulating processes
- B01J2219/00162—Controlling or regulating processes controlling the pressure
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
- C07C15/02—Monocyclic hydrocarbons
- C07C15/067—C8H10 hydrocarbons
- C07C15/08—Xylenes
Definitions
- This present disclosure relates to processes and apparatuses for toluene and benzene methylation in an aromatics complex for producing paraxylene. More specifically, the present disclosure relates to processes and apparatuses for toluene and benzene methylation within an aromatics complex for producing paraxylene wherein an embodiment uses a reactor having a refractory comprising a low iron refractory.
- the xylene isomers are produced in large volumes from petroleum as feedstocks for a variety of important industrial chemicals. The most important of the xylene isomers is para-xylene, the principal feedstock for polyester, which continues to enjoy a high growth rate from large base demand. Ortho-xylene is used to produce phthalic anhydride, which supplies high-volume but relatively mature markets. Meta- xylene is used in lesser but growing volumes for such products as plasticizers, azo dyes and wood preservers. Ethylbenzene generally is present in xylene mixtures and is occasionally recovered for styrene production, but is usually considered a less- desirable component of Cs aromatics.
- Paraxylene is most often produced from a feedstock which has a methyl to phenyl ratio of less than 2. As a result, the paraxylene production is limited by the available methyl groups in the feed. In addition, paraxylene production also typically produces benzene as a byproduct. Since paraxylene is more valuable than benzene and the other byproducts produced in an aromatics complex, there is a desire to maximize the paraxylene production from a given amount of feed.
- Toluene methylation or benzene methylation processes use iron or iron- based alloys as reactor materials. Iron can catalyze the hydrocarbon to form filamentous carbon and thus plug the reactors. Additionally, iron can be corroded through a process called metal dusting when hydrocarbon presents. Coke formation and metal dusting reduce reactor life time and add cost to process operation. The impact can be minimized by lowering the process temperature but this could also bring down the catalyst activity. For fluidized bed, a refractory layer was typically applied inside the vessel to protect metal wall from abrasion. The refractories usually contains some level of iron.
- the iron When exposed to methanol at 600C, the iron can also form metal catalyzed cork and pulverize refractory into small particles. In other cases, if coking is so extreme, the refractory can peel away from the wall and fall into the reactor damaging the internals. This is referred to as‘jacking’. In such case, the refractory cannot be effective any more and may damage other reactor internals.
- the term“stream”,“feed”,“product”,“part” or“portion” can include various hydrocarbon molecules, such as straight-chain, branched, or cyclic alkanes, alkenes, alkadienes, and alkynes, and optionally other substances, such as gases, e.g., hydrogen, or impurities, such as heavy metals, and sulfur and nitrogen compounds.
- hydrocarbon molecules such as straight-chain, branched, or cyclic alkanes, alkenes, alkadienes, and alkynes
- gases e.g., hydrogen, or impurities, such as heavy metals, and sulfur and nitrogen compounds.
- gases e.g., hydrogen, or impurities, such as heavy metals, and sulfur and nitrogen compounds.
- Each of the above may also include aromatic and non-aromatic hydrocarbons.
- Hydrocarbon molecules may be abbreviated Ci, C 2 , C 3 , Cn where“n” represents the number of carbon atoms in the one or more hydrocarbon molecules or the abbreviation may be used as an adjective for, e.g., non-aromatics or compounds.
- aromatic compounds may be abbreviated A 6 , A 7 , As, An where“n” represents the number of carbon atoms in the one or more aromatic molecules.
- a superscript“+” or may be used with an abbreviated one or more hydrocarbons notation, e.g., C 3+ or C 3- , which is inclusive of the abbreviated one or more hydrocarbons.
- the abbreviation“C 3+ ” means one or more hydrocarbon molecules of three or more carbon atoms
- zone can refer to an area including one or more equipment items and/or one or more sub-zones.
- Equipment items can include, but are not limited to, one or more reactors or reactor vessels, separation vessels, distillation towers, heaters, exchangers, pipes, pumps, compressors, and controllers. Additionally, an equipment item, such as a reactor, dryer, or vessel, can further include one or more zones or sub-zones.
- the claimed invention comprises a first embodiment wherein a toluene methylation process or apparatus for alkylating an aromatic hydrocarbon reactant with an alkylating reagent comprising methanol to produce an alkylated aromatic product, comprising a reactor having a refractory.
- the refractory lines the inside of the toluene methylation reactor.
- This invention proposes to apply a layer of special refractory materials on the reactor internal wall.
- the refractory materials has low iron content (less than 0.1 wt%); therefore the coke formation can be dramatically reduced.
- the layer of refractory materials can act as thermal barrier to allow the metal wall stay at lower temperature than the process temperature, thus to further reduce the coke formation on the wall. This can be applied to both fixed bed reactor and fluidized bed reactor.
- the reactor comprises a temperature of 500°C to 700°C.
- the reactor comprises an operating bed density of 0.05 kg/m3 to 0.29 kg/m3.
- the weight hourly space velocity of the reactor is 4 hr- 1 to 20 hr-l .
- the reactor may operate at a pressure of 1 barg to 10 barg.
- the mixed oxide can be applied to a holding structure which is attached to the internal reactor wall. Afterwards the mixed oxide goes through drying and firing process to become rigid and abrasion resistant.
- a first embodiment of the invention is a process for alkylating an aromatic hydrocarbon reactant with an alkylating reagent comprising methanol to produce an alkylated aromatic product, comprising introducing the aromatic hydrocarbon into a reactor having an inner refractory lining having a low iron content; and recovering the alkylate aromatic product, produced by reaction of the aromatic reactant and the alkylating reagent, from the reactor.
- An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the first embodiment in this paragraph, wherein the aromatic hydrocarbon reactant includes toluene, the alkylating reagent includes methanol, and the alkylated aromatic product includes xylene.
- An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the first embodiment in this paragraph, wherein the aromatic hydrocarbon reactant includes benzene, the alkylating reagent includes methanol, and the alkylated aromatic product includes xylene.
- An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the first embodiment in this paragraph, wherein the reactor operates at a temperature of 500°C to 700°C.
- An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the first embodiment in this paragraph, wherein the reactor operates at a pressure of 1 barg to 10 barg.
- An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the first embodiment in this paragraph, wherein the entire inside lining of the reactor is coated with the refractory.
- An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the first embodiment in this paragraph, wherein the refractory comprises a low iron content between 0.0001 wt% to 0.5 wt% iron.
- An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the first embodiment in this paragraph, wherein the refractory comprises a low iron content between 0.0001 wt% to 0.15 wt% iron.
- An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the first embodiment in this paragraph, further comprising adding water to the reactor.
- a second embodiment of the invention is an apparatus for alkylating an aromatic hydrocarbon reactant with an alkylating reagent comprising methanol to produce an alkylated aromatic product, comprising a line comprising the aromatic hydrocarbon in upstream communication with a reactor having an inner refractory lining; and a line in downstream communication with the reactor comprising the alkylate aromatic product, produced by reaction of the aromatic reactant and the alkylating reagent, from the reactor.
- An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the second embodiment in this paragraph, wherein the aromatic hydrocarbon reactant includes toluene, the alkylating reagent includes methanol, and the alkylated aromatic product includes xylene.
- An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the second embodiment in this paragraph, wherein the aromatic
- hydrocarbon reactant includes benzene
- the alkylating reagent includes methanol
- the alkylated aromatic product includes xylene.
- An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the second embodiment in this paragraph, wherein the reactor operates at a temperature of 500°C to 700°C.
- An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the second embodiment in this paragraph, wherein the reactor operates at a pressure of 1 barg to 10 barg.
- An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the second embodiment in this paragraph, wherein the entire inside lining of the reactor is coated with the refractory.
- An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the second embodiment in this paragraph, wherein the refractory comprises a low iron content between 0.0001 wt% to 0.5 wt% iron.
- An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the second embodiment in this paragraph, wherein the refractory comprises a low iron content between 0.0001 to 0.15 wt% iron.
- An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the second embodiment in this paragraph, further comprising an addition line in upstream communication with the reactor comprising water.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Claims
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1020237042519A KR20230173730A (en) | 2018-06-27 | 2019-06-22 | Processes and apparatuses for toluene and benzene methylation in an aromatics complex |
| SG11202012128WA SG11202012128WA (en) | 2018-06-27 | 2019-06-22 | Processes and apparatuses for toluene and benzene methylation in an aromatics complex |
| CN201980039222.5A CN112272660B (en) | 2018-06-27 | 2019-06-22 | Method and apparatus for methylating toluene and benzene in an aromatics complex |
| KR1020207036393A KR20210010570A (en) | 2018-06-27 | 2019-06-22 | Method and apparatus for methylation of toluene and benzene in aromatic complexes |
| CN202310772843.2A CN117024240B (en) | 2018-06-27 | 2019-06-22 | Process and apparatus for the methylation of toluene and benzene in an aromatics complex |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201862690851P | 2018-06-27 | 2018-06-27 | |
| US62/690,851 | 2018-06-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2020005781A1 true WO2020005781A1 (en) | 2020-01-02 |
Family
ID=68987435
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2019/038613 Ceased WO2020005781A1 (en) | 2018-06-27 | 2019-06-22 | Processes and apparatuses for toluene and benzene methylation in an aromatics complex |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US11192833B2 (en) |
| KR (2) | KR20230173730A (en) |
| CN (2) | CN117024240B (en) |
| SG (1) | SG11202012128WA (en) |
| WO (1) | WO2020005781A1 (en) |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104150927A (en) * | 2014-08-06 | 2014-11-19 | 甘肃锦世化工有限责任公司 | Production method for low-iron low-silicon fire-resistant material grade chromium oxide green |
| CN106854128A (en) * | 2016-11-28 | 2017-06-16 | 陕西煤化工技术工程中心有限公司 | A kind of method that toluene produces paraxylene with methyl alcohol |
| WO2018057125A2 (en) * | 2016-09-22 | 2018-03-29 | Exxonmobil Chemical Patents Inc. | Use of light gas by-products in the production of paraxylene by the methylation of toluene and/or benzene |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3182094A (en) | 1961-07-13 | 1965-05-04 | Gulf Research Development Co | Thermal hydrodealkylation process |
| SA94150056B1 (en) * | 1993-01-04 | 2005-10-15 | شيفرون ريسيرتش أند تكنولوجي كمبني | hydrodealkylation |
| US8119203B2 (en) | 2005-06-02 | 2012-02-21 | Chevron Phillips Chemical Company Lp | Method of treating a surface to protect the same |
| US7763766B2 (en) * | 2005-12-22 | 2010-07-27 | Uop Llc | Methanol-to-olefins process with reduced coking |
| CN101808936A (en) * | 2007-07-25 | 2010-08-18 | F.P.C.企业(2008)有限公司 | Chemical process for producing hydrogen chloride and chloride-free complex potassium sulfate fertilizers or other metal sulfates |
| US8197566B2 (en) * | 2008-12-08 | 2012-06-12 | General Electric Company | Gasifier additives for improved refractory life |
| TWI495511B (en) * | 2011-07-27 | 2015-08-11 | Exxonmobil Chem Patents Inc | Fluid bed reactor with staged baffles |
| TW201319254A (en) * | 2011-11-01 | 2013-05-16 | Gevo Inc | Renewable xylenes produced from biological C4 and C5 molecules |
| US9469579B2 (en) * | 2014-06-30 | 2016-10-18 | Exxonmobil Chemical Patents Inc. | Process for the production of xylenes |
-
2019
- 2019-04-08 US US16/377,798 patent/US11192833B2/en active Active
- 2019-06-22 KR KR1020237042519A patent/KR20230173730A/en not_active Ceased
- 2019-06-22 SG SG11202012128WA patent/SG11202012128WA/en unknown
- 2019-06-22 CN CN202310772843.2A patent/CN117024240B/en active Active
- 2019-06-22 KR KR1020207036393A patent/KR20210010570A/en not_active Ceased
- 2019-06-22 WO PCT/US2019/038613 patent/WO2020005781A1/en not_active Ceased
- 2019-06-22 CN CN201980039222.5A patent/CN112272660B/en active Active
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104150927A (en) * | 2014-08-06 | 2014-11-19 | 甘肃锦世化工有限责任公司 | Production method for low-iron low-silicon fire-resistant material grade chromium oxide green |
| WO2018057125A2 (en) * | 2016-09-22 | 2018-03-29 | Exxonmobil Chemical Patents Inc. | Use of light gas by-products in the production of paraxylene by the methylation of toluene and/or benzene |
| CN106854128A (en) * | 2016-11-28 | 2017-06-16 | 陕西煤化工技术工程中心有限公司 | A kind of method that toluene produces paraxylene with methyl alcohol |
Also Published As
| Publication number | Publication date |
|---|---|
| CN117024240A (en) | 2023-11-10 |
| SG11202012128WA (en) | 2021-01-28 |
| US11192833B2 (en) | 2021-12-07 |
| CN112272660B (en) | 2023-07-28 |
| KR20230173730A (en) | 2023-12-27 |
| CN112272660A (en) | 2021-01-26 |
| KR20210010570A (en) | 2021-01-27 |
| CN117024240B (en) | 2025-10-03 |
| US20200002245A1 (en) | 2020-01-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US8598395B2 (en) | Process for increasing a mole ratio of methyl to phenyl | |
| US8609917B2 (en) | Process for increasing methyl to phenyl mole ratios and reducing benzene content in a motor fuel product | |
| US20180170841A1 (en) | Processes and apparatuses for toluene methylation in an aromatics complex | |
| WO2018118675A1 (en) | Processes and apparatuses for toluene methylation in an aromatics complex | |
| US20180170828A1 (en) | Processes and apparatuses for toluene methylation in an aromatics complex | |
| US8734737B2 (en) | Production of EB from toluene and methane | |
| JP5638013B2 (en) | Hydrocarbon dehydrogenation method | |
| US11192833B2 (en) | Processes and apparatuses for toluene and benzene methylation in an aromatics complex | |
| CN111712478B (en) | Method and apparatus for methylating toluene and benzene in an aromatics complex | |
| US11078133B2 (en) | Aromatic alkylation process | |
| US20190144358A1 (en) | Processes and apparatuses for methylation of aromatics in an aromatics complex | |
| CN111433173B (en) | Method and apparatus for methylating aromatic hydrocarbons in an aromatic hydrocarbon complex | |
| KR102570196B1 (en) | Methods and apparatus for methylation of aromatics in aromatic complexes | |
| PL215313B1 (en) | Method for dehydrogenation of hydrocarbons |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 19826760 Country of ref document: EP Kind code of ref document: A1 |
|
| ENP | Entry into the national phase |
Ref document number: 20207036393 Country of ref document: KR Kind code of ref document: A |
|
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| 122 | Ep: pct application non-entry in european phase |
Ref document number: 19826760 Country of ref document: EP Kind code of ref document: A1 |
|
| WWR | Wipo information: refused in national office |
Ref document number: 1020237042519 Country of ref document: KR |