EP3371131A1 - Process and system for making cyclopentadiene and/or dicyclopentadiene - Google Patents
Process and system for making cyclopentadiene and/or dicyclopentadieneInfo
- Publication number
- EP3371131A1 EP3371131A1 EP16862670.3A EP16862670A EP3371131A1 EP 3371131 A1 EP3371131 A1 EP 3371131A1 EP 16862670 A EP16862670 A EP 16862670A EP 3371131 A1 EP3371131 A1 EP 3371131A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- reactor
- rich fraction
- dcpd
- cpd
- stream
- 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.)
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Classifications
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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
- B01J29/00—Catalysts comprising molecular sieves
- B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
- B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
- B01J29/40—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the pentasil type, e.g. types ZSM-5, ZSM-8 or ZSM-11, as exemplified by patent documents US3702886, GB1334243 and US3709979, respectively
- B01J29/42—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the pentasil type, e.g. types ZSM-5, ZSM-8 or ZSM-11, as exemplified by patent documents US3702886, GB1334243 and US3709979, respectively containing iron group metals, noble metals or copper
- B01J29/44—Noble metals
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- 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
- C07C2/02—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
- C07C2/50—Diels-Alder conversion
- C07C2/52—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
- C07C5/373—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen with simultaneous isomerisation
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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
- B01J2229/00—Aspects of molecular sieve catalysts not covered by B01J29/00
- B01J2229/10—After treatment, characterised by the effect to be obtained
- B01J2229/18—After treatment, characterised by the effect to be obtained to introduce other elements into or onto the molecular sieve itself
- B01J2229/186—After treatment, characterised by the effect to be obtained to introduce other elements into or onto the molecular sieve itself not in framework positions
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2529/00—Catalysts comprising molecular sieves
- C07C2529/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites, pillared clays
- C07C2529/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
- C07C2529/40—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the pentasil type, e.g. types ZSM-5, ZSM-8 or ZSM-11
- C07C2529/42—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the pentasil type, e.g. types ZSM-5, ZSM-8 or ZSM-11 containing iron group metals, noble metals or copper
- C07C2529/44—Noble metals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
- C07C2601/10—Systems containing only non-condensed rings with a five-membered ring the ring being unsaturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/56—Ring systems containing bridged rings
- C07C2603/58—Ring systems containing bridged rings containing three rings
- C07C2603/60—Ring systems containing bridged rings containing three rings containing at least one ring with less than six members
- C07C2603/66—Ring systems containing bridged rings containing three rings containing at least one ring with less than six members containing five-membered rings
- C07C2603/68—Dicyclopentadienes; Hydrogenated dicyclopentadienes
Definitions
- the present invention relates to processes and systems for making cyclic C5s including cyclopendadiene and/or dicyclopentadiene.
- the present invention relates to processes and systems for making cyclopendadiene and dicyclopentadiene from acyclic C5 hydrocarbons.
- Cyclopentadiene (CPD) and its dimer dicyclopentadiene (DCPD) are highly desired raw materials used throughout the chemical industry in a wide range of products such as polymeric materials, polyester resins, synthetic rubbers, solvents, fuels, fuel additives, etc.
- cyclopentadiene is produced as a minor byproduct in liquid fed steam cracking (e.g., naphtha and heavier feed) processes. As steam cracking processes shift to using lighter feed (e.g., ethane and propane feed), less CPD is produced while demand for CPD continues to rise.
- Cyclopentane and cyclopentene also have high value as solvents while cyclopentene may be used as a monomer to produce polymers and as a starting material for other high value chemicals.
- the reaction converting C5 hydrocarbons to CPD is extremely endothermic and is favored by low pressure and high temperature but significant cracking of n-pentane and other C5 hydrocarbons can occur at relatively low temperature (e.g., 450°C-500°C).
- Other challenges include loss of catalyst activity due to coking during the production process and further processing is needed to remove coke from the catalyst, and the inability to use oxygen-containing gas to directly provide heat input to the reactor without damaging the catalyst.
- DCPD is easier to handle than CPD as a feed material for subsequent chemical syntheses.
- DCPD and CPD are fungible in many applications. In certain applications DCPD is preferably used directly in lieu of CPD. For other applications where CPD is needed, DCPD can be thermally depolymerized (aka cracked) via retro-Diels-Alder reaction to CPD at the point of use.
- CPD C5 hydrocarbon stream(s) comprising CPD at a modest concentration, acyclic diolefins at significant concentrations, and mono olefins. Because many of the C5 species have close boiling points, form azeotropes, and are reactive at distillation temperatures, CPD recovery from the product mixture via conventional distillation is not industrially feasible. In conventional recovery schemes, CPD is recovered from other C5 hydrocarbons utilizing dimerization process(es) which causes CPD to undergo Diels-Alder reaction to produce DCPD that can easily be separated from the C5 hydrocarbons by conventional distillation.
- CPD can also react with other diolefins present in the stream to produce co-dimers, which contaminate the DCPD.
- reactions involving higher-order oligomers also occur at moderate to high temperatures.
- These side reactions produce undesirable co-dimers and higher-order oligomers, which necessitate more downstream processing steps, such as repeated, multi-step cracking and dimerization, to produce DCPD with sufficient purity required for many applications.
- Such processes are expensive, low in yield, and can be prone to fouling.
- a first aspect of the present invention relates to a process for making cyclic C5s including CPD and/or DCPD comprising: (I) feeding a C5 feedstock comprising at least one acyclic C5 hydrocarbon into a first reactor; (II) contacting the at least one acyclic C5 hydrocarbon with a catalyst under conversion conditions to obtain a first reactor hydrocarbon effluent comprising: C5 components including CPD and acyclic diolefins; light components including hydrogen and C1-C4 hydrocarbons; one-ring aromatics; and multiple-ring aromatics; and (III) separating the first reactor hydrocarbon effluent to produce (i) a light components-rich fraction and (ii) a first C5-rich fraction comprising CPD.
- High-purity DCPD can be produced from the first C5-rich fraction, which can contain CPD, by dimerization.
- a second aspect of the present invention relates to a system for making cyclic C5s including CPD and/or DCPD, comprising: (A) a first reactor configured to receive a C5 feedstock comprising at least one acyclic C5 hydrocarbon, an optional hydrogen co-feedstock and an optional C1-C4 hydrocarbon co-feedstock; (B) a catalyst loaded inside the first reactor capable of catalyzing the conversion of the acyclic C5 hydrocarbon under conversion conditions to produce a first reactor hydrocarbon effluent comprising: C5 components including CPD and acyclic diolefins; light components including hydrogen and C1-C4 hydrocarbons; one-ring aromatics; and multiple-ring aromatics; and (C) a first separation subsystem in direct or indirect fluid communication with the first reactor configured to receive at least a portion of the first reactor hydrocarbon effluent and to produce (i) a first C5-rich fraction comprising CPD and depleted of hydrogen and C1-C4 hydrocarbons and (i
- FIG. 1 is a schematic illustration of an exemplary process and system for making CPD and/or DCPD of the present invention.
- FIG. 2 is a schematic illustration of the details of the first separation sub-system in FIG. 1.
- each step is an action or operation that may be carried out once or multiple times in the process, in a continuous or discontinuous fashion.
- each of the steps in a process may be conducted sequentially in the order as they are listed, with or without overlapping with one or more other steps, or in any other order, as the case may be.
- one or more or even all steps may be conducted simultaneously with regard to the same or different batch of material.
- a second step may be carried out simultaneously with respect to an intermediate material resulting from treating the raw materials fed into the process at an earlier time in the first step.
- the steps are conducted in the order described.
- cyclic C5" or "cC5" includes, but is not limited to, cyclopentane, cyclopentene, cyclopentadiene, and mixtures of two or more thereof.
- cyclic Cs or “cCs” also includes alkylated analogs of any of the foregoing, e.g., methyl cyclopentane, methyl cyclopentene, and methyl cyclopentadiene. It should be recognized for purposes of the invention that cyclopentadiene spontaneously dimerizes over time to form dicyclopentadiene via Diels-Alder condensation over a range of conditions, including ambient temperature and pressure.
- acyclic includes, but is not limited to, linear and branched saturates and non-saturates.
- aromatic means a planar cyclic hydrocarbyl with conjugated double bonds, such as benzene.
- aromatic encompasses compounds containing one or more aromatic rings, including, but not limited to, benzene, toluene and xylene and polynuclear aromatics (PNAs) which include, but are not limited to, naphthalene, anthracene, chrysene, and their alkylated versions.
- C6+ aromatics includes compounds based upon an aromatic ring having six or more ring atoms, including, but not limited to, benzene, toluene and xylene and polynuclear aromatics (PNAs) which include, but are not limited to, naphthalene, anthracene, chrysene, and their alkylated versions.
- PNAs polynuclear aromatics
- BTX includes, but is not limited to, a mixture of benzene, toluene, and xylene (ortho and/or meta and/or para).
- a component in a given mixture or stream produced from a predecessor mixture or stream means that the component is present at a non-negligible concentration in the given mixture or stream that is higher than its concentration in the predecessor mixture or stream.
- a C5-rich fraction produced from a predecessor stream is a fraction comprising C5 hydrocarbons at a non-negligible concentration that is higher than the concentration of C5 hydrocarbons in the predecessor stream.
- a hydrogen-depleted fraction produced from a predecessor stream is a fraction comprising hydrogen at a concentration (which can be negligible) that is lower than the concentration of hydrogen in the predecessor stream.
- wt% means percentage by weight
- vol% means percentage by volume
- mol% means percentage by mole
- An "upper stream” as used herein may be at the very top or the side of a vessel such as a fractionation column or a reactor, with or without an additional stream above it.
- an upper stream is drawn at a location in the vicinity of the top of the column.
- an upper stream is drawn at a location above at least one feed.
- a "lower stream” as used herein is at a location lower than the upper stream, which may be at the very bottom or the side of a vessel, and if at the side, with or without an additional stream below it.
- a lower stream is drawn at a location in the vicinity of the bottom of the column.
- a lower stream is drawn at a location below at least one feed.
- a "middle stream” is a stream between an upper stream and a lower stream.
- light hydrocarbons means hydrocarbons comprising 1 to 4 carbon atoms in their molecule structures.
- light components means hydrogen and hydrocarbons comprising 1 to 4 carbon atoms in their molecule structures.
- hydrogen means molecular H2.
- normal boiling point means boiling point under a pressure of 101 kilopascal.
- vapor and gas are both inclusive to mean a phase that is entirely vapor, entirely gas and mixtures of gas and vapor.
- the term "essentially free of means comprising at a concentration not higher than 1 wt%, e.g., ⁇ 0.8 wt%, ⁇ 0.6 wt%, ⁇ 0.5 wt%, ⁇ 0.1 wt%, ⁇ 0.01 wt%, or even ⁇ 0.001 wt%.
- mogas means a mixture of organic compounds suitable as fuel for use in gasoline internal combustion engine.
- coke includes, but is not limited to, a low hydrogen content hydrocarbon that is adsorbed on the catalyst composition.
- Cn means hydrocarbon(s) having n carbon atom(s) per molecule, wherein n is a positive integer.
- a C5 hydrocarbon feedstock therefore, comprises one or more hydrocarbon, saturated or unsaturated, having 5 carbon atoms per molecule, such as n-pentane, 2-methyl-butane, 2,2-dimethylpentane, 1-pentene, 2-pentene, 2-methyl-2-butene, 3-methyl-2-butene,l ,3-pentadiene, 1 ,4-pentadiene, 2-methy 1-1 , 3 -butadiene, cyclopentane, cyclopentene, and the like.
- Cn+ means hydrocarbon(s) having at least n carbon atom(s) per molecule.
- Cn- means hydrocarbon(s) having no more than n carbon atom(s) per molecule.
- hydrocarbon means a class of compounds containing hydrogen bonded to carbon, and encompasses (i) saturated hydrocarbon compounds, (ii) unsaturated hydrocarbon compounds, and (iii) mixtures of hydrocarbon compounds (saturated and/or unsaturated), including mixtures of hydrocarbon compounds having different values of n.
- C5 feedstock includes a feedstock containing n-pentane, such as a feedstock which is predominately normal pentane (n-pentane) and/or isopentane (also referred to as methylbutane), with smaller fractions of cyclopentane and/or neopentane (also referred to as 2,2-dimethylpropane).
- n-pentane predominately normal pentane
- isopentane also referred to as methylbutane
- 2,2-dimethylpropane also referred to as 2,2-dimethylpropane
- one-ring aromatics means aromatic compounds having one benzene ring in the molecular structures thereof and includes alkylated versions thereof such as toluene, xylenes, and ethylbenzene.
- multiple-ring aromatics means aromatic compounds having two or more aromatic rings in the molecular structures thereof and includes alkylated versions thereof.
- Group 10 metal means an element in Group 10 of the Periodic Table and includes Ni, Pd, and Pt.
- Group 1 alkali metal means an element in Group 1 of the Periodic Table and includes, but is not limited to, Li, Na, K, Rb, Cs, and a mixture of two or more thereof, and excludes hydrogen.
- Group 2 alkaline earth metal means an element in Group 2 of the Periodic Table and includes, but is not limited to, Be, Mg, Ca, Sr, Ba, and a mixture of two or more thereof.
- Group 11 metal means an element in Group 11 of the Periodic Table and includes, but is not limited to, Cu, Ag, Au, and a mixture of two or more thereof.
- molecular sieve of the MCM-22 family includes one or more of:
- molecular sieves made from a common first degree crystalline building block unit cell, which unit cell has the MWW framework topology.
- a unit cell is a spatial arrangement of atoms which if tiled in three-dimensional space describes the crystal structure. Such crystal structures are discussed in the "Atlas of Zeolite Framework Types", Fifth edition, 2001, the entire content of which is incorporated as reference);
- molecular sieves made from a common second degree building block, being a 2-dimensional tiling of such MWW framework topology unit cells, forming a monolayer of one unit cell thickness, preferably one c-unit cell thickness;
- molecular sieves made from common second degree building blocks, being layers of one or more than one unit cell thickness, wherein the layer of more than one unit cell thickness is made from stacking, packing, or binding at least two monolayers of one unit cell thickness.
- the stacking of such second degree building blocks may be in a regular fashion, an irregular fashion, a random fashion, or any combination thereof;
- molecular sieves made by any regular or random 2-dimensional or 3-dimensional combination of unit cells having the MWW framework topology.
- the MCM-22 family includes those molecular sieves having an X-ray diffraction pattern including d-spacing maxima at 12.4 ⁇ 0.25, 6.9 ⁇ 0.15, 3.57 ⁇ 0.07, and 3.42 ⁇ 0.07 Angstrom.
- the X-ray diffraction data used to characterize the material are obtained by standard techniques using the K-alpha doublet of copper as incident radiation and a diffractometer equipped with a scintillation counter and associated computer as the collection system.
- molecular sieve is used synonymously with the term “microporous crystalline material.”
- carbon selectivity means the moles of carbon in the respective cyclic C5, CPD, CI, and C2-4 formed divided by total moles of carbon in the C5 feedstock converted.
- carbon selectivity to cyclic C5 of at least 30% means that 30 moles of carbon in the cyclic C5 is formed per 100 moles of carbon in the C5 feedstock (such as n-pentane) converted.
- conversion means the moles of carbon in the acyclic C5 hydrocarbon(s) that is converted to a product.
- conversion of at least 70% of said acyclic C5 hydrocarbon(s) to a product means that at least 70% of the moles of said acyclic C5 hydrocarbon(s) was converted to a product.
- ferrilicate means an iron-containing microporous crystalline structure that contains iron in the framework structure and/or in the channel system.
- alkylated naphthalene(s) includes monoalkyl, dialkyl, trialkyl, and tetraalkyl naphthalenes.
- a C5 feedstock comprising acyclic C5 hydrocarbon(s) useful herein is obtainable from crude oil or natural gas condensate, can include virgin C5, and can include cracked C5 (in various degrees of unsaturation: alkenes, dialkenes, alkynes) produced by refining and chemical processes, such as fluid catalytic cracking (FCC), reforming, hydrocracking, hydrotreating, coking, and steam cracking.
- FCC fluid catalytic cracking
- the C5 feedstock useful in the process of this invention comprises pentane, pentene, pentadiene and mixtures of two or more thereof.
- the C5 feedstock comprises at least about 50 wt%, or 60 wt%, or 75 wt%, or 90 wt% saturated acyclic C5 hydrocarbon(s), ideally n-pentane, or in the range from about 50 wt% to about 100 wt% saturated acyclic C5 hydrocarbon(s), ideally n-pentane.
- 2- methylbutane is present at less than 10 wt%.
- the C5 feedstock optionally, does not comprise C6 aromatic compounds, such as benzene.
- C6 aromatic compounds are present at less than 5 wt%, or less than 1 wt%, or less than 0.01 wt%, or even 0 wt%.
- the C5 feedstock optionally, does not comprise toluene and/or one or more of the xylenes (ortho, meta, and para).
- toluene and xylenes are present in the C5 feedstock at less than 5 wt%, preferably less than 1 wt%, preferably present at less than 0.01 wt%, preferably at 0 wt%.
- the C5 feedstock optionally, does not comprise C6+ aromatic compounds, preferably C6+ aromatic compounds are present at less than 5 wt%, preferably less than 1 wt%, preferably present at less than 0.01 wt%, preferably at 0 wt%.
- the C5 feedstock optionally, does not comprise C6+ compounds, preferably C6+ compounds are present at less than 5 wt%, preferably less than 1 wt%, preferably present at less than 0.01 wt%, preferably at 0 wt%, preferably any C6+ aromatic compounds are present at less than 5 wt%, preferably less than 1 wt%, preferably present at less than 0.01 wt%, preferably at 0 wt%.
- the acyclic C5 hydrocarbon(s) contained in the C5 feedstock is fed into a first reactor loaded with a catalyst, where the acyclic C5 hydrocarbons contact the catalyst under conversion conditions, whereupon at least a portion of the acyclic C5 hydrocarbon(s) molecules are converted into CPD molecules, and a reaction product containing CPD and, optionally, other cyclic hydrocarbons (e.g., C5 cyclic hydrocarbons such as cyclopentane and cyclopentene) exits the first reactor as a first reactor hydrocarbon effluent.
- C5 cyclic hydrocarbons such as cyclopentane and cyclopentene
- a hydrogen co-feedstock comprising hydrogen and, optionally, light hydrocarbons, such as C1-C4 hydrocarbons, is also fed into the first reactor.
- at least a portion of the hydrogen co-feedstock is admixed with at least a portion, preferably the entirety, of the C5 feedstock prior to being fed into the first reactor. The presence of hydrogen in the feed mixture at the inlet location, where the feed first comes into contact with the catalyst, prevents or reduces the formation of coke on the catalyst particles.
- the catalyst composition which is described in greater detail below, may comprise a microporous crystalline metallosilicate, preferably having a constraint index in the range of less than 12, a Group 10 metal in combination with a Group 1 alkali metal and/or a Group 2 alkaline earth metal; and, optionally, a Group 11 metal.
- the catalyst can be made by using a method described in greater detail below.
- the first reactor can be a plug flow reactor or other reactor configurations.
- the catalyst can be loaded as a fixed bed, a catalyst particle fluid, and the like.
- the term "reactor" refers to any vessel(s) in which a chemical reaction occurs. Reactor includes both distinct reactors as well as reaction zones within a single reactor apparatus and, as applicable, reaction zones across multiple reactors. In other words and as is common, a single reactor may have multiple reaction zones. Where the description refers to a first and second reactor, the person of ordinary skill in the art will readily recognize such reference includes two reactors, as well as a single reactor having first and second reaction zones. Likewise, a first reactor hydrocarbon effluent and a second reactor effluent will be recognized to include the effluent from the first reaction zone and the second reaction zone of a single reactor, respectively.
- the term "moving bed” reactor refers to a zone or vessel with contacting of solids (e.g., catalyst particles) and gas flows such that the superficial gas velocity (U) is below the velocity required for dilute-phase pneumatic conveying of solid particles in order to maintain a solids bed with void fraction below 95%.
- the solids e.g., catalyst material
- the solids may slowly travel through the reactor and may be removed from the bottom of the reactor and added to the top of the reactor.
- a moving bed reactor may operate under several flow regimes including settling or moving packed-bed regime (U ⁇ Umf), bubbling regime (Umf ⁇ U ⁇ Umb), slugging regime (Umb ⁇ U ⁇ U c ), transition to and turbulent fluidization regime (U c ⁇ U ⁇ Utr), and fast-fluidization regime (U>Utr), where Umf is minimum fluidizing velocity, Umb is minimum bubbling velocity, U c is the velocity at which fluctuation in pressure peaks, and Utr is transport velocity.
- These different fluidization regimes have been described in, for example, Kunii, D., Levenspiel, O., Chapter 3 of Fluidization Engineering, 2 nd Edition, Butterworth-Heinemann, Boston, 1991 and Walas, S. M., Chapter 6 of Chemical Process Equipment, Revised 2 nd Edition, Butterworth-Heinemann, Boston, 2010, which are incorporated by reference herein.
- the term "settling bed" reactor refers to a zone or vessel wherein particulates contact with gas flows such that the superficial gas velocity (U) is below the minimum velocity required to fluidize the solid particles (e.g., catalyst particles), the minimum fluidization velocity (Umf), U ⁇ Umf, in at least a portion of the reaction zone, and/or operating at a velocity higher than the minimum fluidization velocity while maintaining a gradient in gas and/or solid property (such as, temperature, gas or solid composition, etc.) axially up the reactor bed by using reactor internals to minimize gas-solid, back-mixing.
- the minimum fluidization velocity is given in, for example, Kunii, D., Levenspiel, O., Chapter 3 of Fluidization Engineering, 2 nd Edition, Butterworth-Heinemann,
- a settling bed reactor may be a "circulating settling bed reactor,” which refers to a settling bed with a movement of solids (e.g., catalyst material) through the reactor and at least a partial recirculation of the solids (e.g., catalyst material).
- the solids e.g., catalyst material
- the solids may have been removed from the reactor, regenerated, reheated and/or separated from the product stream and then returned back to the reactor.
- the term "fluidized bed” reactor refers to a zone or vessel with contacting of solids (e.g., catalyst particles) and gas flows such that the superficial gas velocity (U) is sufficient to fluidize solid particles (i.e., above the minimum fluidization velocity Umf) and is below the velocity required for dilute-phase pneumatic conveying of solid particles in order to maintain a solids bed with void fraction below 95%.
- solids e.g., catalyst particles
- Umf the superficial gas velocity
- cascaded fluid-beds means a series arrangement of individual fluid-beds such that there can be a gradient in gas and/or solid property (such as, temperature, gas or solid composition, pressure, etc.) as the solid or gas cascades from one fluid-bed to another.
- a fluidized bed reactor may be a moving fluidized bed reactor, such as a "circulating fluidized bed reactor,” which refers to a fluidized bed with a movement of solids (e.g., catalyst material) through the reactor and at least a partial recirculation of the solids (e.g., catalyst material).
- the solids e.g., catalyst material
- the solids may have been removed from the reactor, regenerated, reheated and/or separated from the product stream and then returned back to the reactor.
- the term "riser” reactor also known as a transport reactor refers to a zone or vessel (such as, vertical cylindrical pipe) used for net upwards transport of solids (e.g., catalyst particles) in fast-fluidization or pneumatic conveying fluidization regimes.
- Fast fluidization and pneumatic conveying fluidization regimes are characterized by superficial gas velocities (U) greater than the transport velocity (Utr).
- U superficial gas velocities
- Utr transport velocity
- Fast fluidization and pneumatic conveying fluidization regimes are also described in Kunii, D., Levenspiel, O., Chapter 3 of Fluidization Engineering, 2 nd Edition, Butterworth-Heinemann, Boston, 1991 and Walas, S. M., Chapter 6 of Chemical Process Equipment, Revised 2 nd Edition, Butterworth-Heinemann, Boston, 2010.
- a fluidized bed reactor such as a circulating fluidized bed reactor, may be operated as a riser reactor.
- co-current refers to a flow of two streams (e.g., stream
- stream (b)) in substantially the same direction.
- stream (a) flows from a top portion to a bottom portion of at least one reaction zone and stream (b) flows from a top portion to a bottom portion of at least one reaction zone
- the flow of stream (a) would be considered co-current to the flow of stream (b).
- counter-current refers to a flow of two streams (e.g., stream (a), stream (b)) in substantially opposing directions. For example, if stream (a) flows from a top portion to a bottom portion of the at least one reaction zone and stream (b) flows from a bottom portion to a top portion of the at least one reaction zone, the flow of stream (a) would be considered counter-current to the flow of stream (b). On a smaller scale within the reaction zone, there may be regions where flow may not be counter-current.
- the process for the conversion of an acyclic C5 hydrocarbon to a product comprising cyclic C5 compounds comprises contacting the C5 feedstock and, optionally, hydrogen under acyclic C5 conversion conditions in the presence of one or more catalyst compositions, including but not limited to the catalyst compositions described herein, to form said product.
- the product of the process for conversion of an acyclic C5 feedstock comprises cyclic C5 compounds.
- the cyclic C5 compounds can comprise one or more of cyclopentane, cyclopentene, cyclopentadiene, and includes mixtures thereof.
- the acyclic C5 conversion conditions include at least a temperature, a partial pressure, and a weight hourly space velocity (WHSV).
- the temperature is in the range of about 400°C to about 700°C, or in the range from about 450°C to about 650°C, preferably, in the range from about 500°C to about 600°C.
- the partial pressure is in the range of about 3 to about 100 psi (21 to 689 kilopascal), or in the range from about 3 to about 50 psi (21 to 345 kilopascal), preferably, in the range from about 3 to about 20 psi (21 to 138 kilopascal).
- the weight hourly space velocity is in the range from about 1 to about 50 hr 1 , or in the range from about 1 to about 20 hr 1 .
- Such conditions include a molar ratio of the optional hydrogen co-feed to the acyclic C5 hydrocarbon in the range of about 0 to 3, or in the range from about 0.5 to about 2.
- Such conditions may also include co-feed C1-C4 hydrocarbons with the acyclic C5 feed.
- this invention relates to a process for conversion of n-pentane to cyclopentadiene comprising the steps of contacting n-pentane and, optionally, hydrogen (if present, typically H2 is present at a molar ratio of hydrogen to n-pentane of 0.01 to 3.0) with one or more catalyst compositions including, but not limited to, the catalyst compositions described herein, to form cyclopentadiene at a temperature of 400°C to 700°C, a partial pressure of 3 to about 100 psia, and a weight hourly space velocity of 1 to about 50 hr 1 .
- a number of desired and undesirable side reactions may take place. The net effect of the reactions is the production of hydrogen and the increase of total volume (assuming constant total pressure).
- One particularly desired overall reaction i.e., intermediate reaction steps are not shown) is:
- Fluids inside the first reactor are essentially in gas phase.
- a first reactor hydrocarbon effluent preferably in gas phase, is obtained.
- the first reactor hydrocarbon effluent may comprise a mixture of the following hydrocarbons, among others: heavy components comprising more than 8 carbon atoms such as multiple-ring aromatics; C8, C7, and C6 hydrocarbons such as one-ring aromatics; CPD (the desired product); unreacted C5 feedstock material such as n-pentane; C5 by-products such as pentenes
- the first reactor hydrocarbon effluent may comprise CPD at a concentration of C(CPD)1 wt%, based on the total weight of the C5 hydrocarbons in the first reactor hydrocarbon effluent; and al ⁇ C(CPD)1 ⁇ a2, where al and a2 can be, independently, 15, 16, 18, 20, 22, 24, 25, 26, 28, 30, 32, 34, 35, 36, 38, 40, 45, 50, 55, 60, 65, 70, 75, 80, or 85 as long as al ⁇ a2.
- the first reactor hydrocarbon effluent may comprise acyclic diolefins at a total concentration of C(ADO)l wt%, based on the total weight of the C5 hydrocarbons in the first reactor hydrocarbon effluent; and bl ⁇ C(ADO)l ⁇ b2, where bl and b2 can be, independently, 20, 18, 16, 15, 14, 12, 10, 8, 6, 5, 4, 3, 2, 1, or 0.5, as long as bl ⁇ b2. Preferably, 0.5 ⁇ C(ADO) ⁇ 10.
- the acyclic diolefins comprise 1,3-pentadiene at a concentration of C(PTD)1 wt%, based on the total weight of C5 components in the first reactor hydrocarbon effluent; and cl ⁇ C(PTD)1 ⁇ c2, where cl and c2 can be, independently, 20, 18, 16, 15, 14, 12, 10, 8, 6, 5, 4, 3, 2, 1, 0.5, or 0.3, as long as cl ⁇ c2.
- a high CPD to acyclic diolefin molar ratio in the first reactor hydrocarbon effluent can be achieved such that C(CPD)l/C(ADO)l > 1.5, preferably 1.6, 1.8, 2.0, 2.2, 2.4, 2.5, 2.6, 2.8, 3.0, 3.2, 3.4, 3.5, 3.6, 3.8, 4.0, 5.0, 6.0, 8.0, 10, 12, 14, 15, 16, 18, or 20.
- the high ratio of C(CPD)l/C(ADO)l significantly reduces CPD loss as a result of Diels-Alder reactions between CPD and acyclic dienes in subsequent processing steps, and therefore, allows the processes of the present invention to achieve high DCPD yield and high DCPD purity for the subsequently produced DCPD fractions.
- the total absolute pressure and temperature of the first reactor hydrocarbon effluent should be maintained at levels such that the dimerization of CPD to form DCPD is substantially avoided, and the Diels-Alder reactions between CPD and acyclic dienes are substantially inhibited.
- Catalyst compositions useful herein include microporous crystalline metallosilicates, such as crystalline aluminosilicates, crystalline ferrosilicates, or other metal containing crystalline silicates (such as those where the metal or metal containing compound is dispersed within the crystalline silicate structure and may or may not be a part of the crystalline framework).
- microporous crystalline metallosilicate framework types useful as catalyst compositions herein include, but are not limited to, MWW, MFI, LTL, MOR, BEA, TON, MTW, MTT, FER, MRE, MFS, MEL, DDR, EUO, and FAU.
- microporous metallosilicates for use herein include those of framework type MWW, MFI, LTL, MOR, BEA, TON, MTW, MTT, FER, MRE, MFS, MEL, DDR, EUO, and FAU where one or more metals from groups 8, 11, and 13 of the Periodic Table of the Elements (preferably one or more of Fe, Cu, Ag, Au, B, Al, Ga, and/or In) are incorporated in the crystal structure during synthesis or impregnated post crystallization.
- a metallosilicate may have one or more metals present and, for example, a material may be referred to as a ferrosilicate, but it will most likely still contain small amounts of aluminum.
- the microporous crystalline metallosilicates preferably have a constraint index of less than 12, alternately from 1 to 12, alternately from 3 to 12.
- Aluminosilicates useful herein have a constraint index of less than 12, such as 1 to 12, alternately 3 to 12, and include, but are not limited to Zeolite beta, mordenite, faujasite, Zeolite L, ZSM-5, ZSM-11, ZSM-22, ZSM-23, ZSM-35, ZSM-48, ZSM-50, ZSM-57, ZSM-58, MCM-22 family materials, and mixtures of two or more thereof.
- the microporous crystalline aluminosilicate has a constraint index of about 3 to about 12 and is ZSM-5.
- ZSM-5 is described in US 3,702,886.
- ZSM-11 is described in US 3,709,979.
- ZSM-22 is described in US 5,336,478.
- ZSM-23 is described in US 4,076,842.
- ZSM-35 is described in US 4,016,245.
- ZSM-48 is described in US 4,375,573.
- ZSM-50 is described in US 4,640,829, and ZSM-57 is described in US 4,873,067.
- ZSM-58 is described in US 4,698,217. Constraint index and a method for its determination are described in US 4,016,218. The entire contents of each of the aforementioned patents are incorporated herein by reference.
- the MCM-22 family material is selected from the group consisting of MCM-22, PSH-3, SSZ-25, MCM-36, MCM-49, MCM-56, ERB-1, EMM-10, EMM-10-P, EMM-12, EMM-13, UZM-8, UZM-8HS, ITQ-1, ITQ-2, ITQ-30, and mixtures of two or more thereof.
- Materials of the MCM-22 family include MCM-22 (described in US 4,954,325), PSH-3 (described in US 4,439,409), SSZ-25 (described in US 4,826,667), ERB-1 (described in EP 293 032), ITQ-1 (described in US 6,077,498), and ITQ-2 (described in WO 97/17290), MCM-36 (described in US 5,250,277), MCM-49 (described in US 5,236,575), MCM-56 (described in US 5,362,697), and mixtures of two or more thereof.
- zeolites to be included in the MCM-22 family are UZM-8 (described in US 6,756,030) and UZM-8HS (described in US 7,713,513), both of which are also suitable for use as the molecular sieve of the MCM-22 family.
- the microporous crystalline metallosilicate has an Si/M molar ratio greater than about 3, or greater than about 25, or greater than about 50, or greater than about 100, or greater than 400, or in the range from about 100 to about 2,000, or from about 100 to about 1,500, or from about 50 to 2,000, or from about 50 to 1,200.
- the microporous crystalline aluminosilicate has an
- Si02/A1203 molar ratio greater than about 3, or greater than about 25, or greater than about
- the microporous crystalline metallosilicate (such as an aluminosilicate) is combined with a Group 10 metal or metal compound, and, optionally, one, two, three, or more Group 1, 2, or 11 metals or metal compounds.
- the Group 10 metal includes, or is selected from the group consisting of, Ni, Pd, and Pt, preferably Pt.
- the Group 10 metal content of said catalyst composition is at least 0.005 wt%, based on the weight of the catalyst composition. In one or more embodiments, the Group 10 content is in the range from about 0.005 wt% to about 10 wt%, or from about 0.005 wt% up to about 1.5 wt%, based on the weight of the catalyst composition.
- the Group 1 alkali metal includes, or is selected from the group consisting of, Li, Na, K, Rb, Cs, and mixtures of two or more thereof, preferably Na.
- the Group 2 alkaline earth metal is selected from the group consisting of Be, Mg, Ca, Sr, Ba, and mixtures of two or more thereof.
- the Group 1 alkali metal is present as an oxide and the metal is selected from the group consisting of Li, Na, K, Rb, Cs, and mixtures of two or more thereof.
- the Group 2 alkaline earth metal is present as an oxide and the metal is selected from the group consisting of Be, magnesium, calcium Sr, Ba, and mixtures of two or more thereof.
- the Group 1 alkali metal is present as an oxide and the metal is selected from the group consisting of Li, Na, K, Rb, Cs, and mixtures of two or more thereof; and the Group 2 alkaline earth metal is present as an oxide and the metal is selected from the group consisting of Be, Mg, Ca, Sr, Ba, and mixtures of two or more thereof.
- the Group 11 metal includes, or is selected from the group consisting of, silver, gold, copper, preferably silver or copper.
- the Group 11 metal content of said catalyst composition is at least 0.005 wt%, based on the weight of the catalyst composition. In one or more embodiments, the Group 11 content is in the range from about 0.005 wt% to about 10 wt%, or from about 0.005 wt% up to about 1.5 wt%, based on the weight of the catalyst composition.
- the catalyst composition has an Alpha Value (as measured prior to the addition of the Group 10 metal, preferably platinum) of less than 25, alternately less than 15, alternately from 1 to 25, alternately from 1.1 to 15.
- the molar ratio of said Group 1 alkali metal to Al is at least about 0.5, or from at least about 0.5 up to about 3, preferably at least about 1, more preferably at least about 2.
- the molar ratio of said Group 2 alkaline earth metal to Al is at least about 0.5, or from at least about 0.5 up to about 3, preferably at least about 1, more preferably at least about 2.
- the molar ratio of said Group 11 metal to Group 10 metal is at least about 0.1, or from at least about 0.1 up to about 10, preferably at least about 0.5, more preferably at least about 1.
- the Group 11 alkaline earth metal is present as an oxide and the metal is selected from the group consisting of gold, silver, and copper, and mixtures of two or more thereof.
- catalyst compositions useful herein are employed at conversion conditions, including a temperature in the range of from 400 to 800°C, a pressure in the range of from 10 to 1,000 kilopascal absolute, and a WHSV in the range of 1 to 100 hr 1 .
- the use of the catalyst compositions of this invention provides a conversion of at least about 60%, or at least about 75%, or at least about 80%, or in the range from about 60% to about 80%, of said acyclic C5 feedstock under acyclic C5 conversion conditions of an n-pentane containing feedstock with equimolar H 2 , a temperature in the range of about 550°C to about 600°C, an n-pentane partial pressure between 3 and 10 psia, and an n-pentane weight hourly space velocity of 10 to 20 hr 1 .
- any one of the catalyst compositions of this invention provides a carbon selectivity to cyclic C5 compounds of at least about 30%, or at least about 40%, or at least about 50%, or in the range from about 30% to about 80%, under acyclic C5 conversion conditions including an n-pentane feedstock with equimolar t3 ⁇ 4, a temperature in the range of about 550°C to about 600°C, an n-pentane partial pressure between 3 and 10 psia, and an n-pentane weight hourly space velocity between 10 and 20 hr 1 .
- any one of the catalyst compositions of this invention provides a carbon selectivity to cyclopentadiene of at least about 30%, or at least about 40%, or at least about 50%, or in the range from about 30% to about 80%, under acyclic C5 conversion conditions including an n-pentane feedstock with equimolar t3 ⁇ 4, a temperature in the range of about 550°C to about 600°C, an n-pentane partial pressure between 3 and 10 psia, and an n-pentane weight hourly space velocity between 10 and 20 hr 1 .
- the catalyst compositions of this invention can be combined with a matrix or binder material to render them attrition resistant and more resistant to the severity of the conditions to which they will be exposed during use in hydrocarbon conversion applications.
- the combined compositions can contain 1 to 99 wt% of the materials of the invention based on the combined weight of the matrix (binder) and material of the invention.
- the relative proportions of microcrystalline material and matrix may vary widely, with the crystal content ranging from about 1 to about 90 wt% and more usually, particularly when the composite is prepared in the form of beads, extrudates, pills, oil drop formed particles, spray dried particles, etc., in the range of about 2 to about 80 wt% of the composite.
- coke may be deposited on the catalyst compositions, whereby such catalyst compositions lose a portion of its catalytic activity and become deactivated.
- the deactivated catalyst compositions may be regenerated by conventional techniques including high pressure hydrogen treatment and combustion of coke on the catalyst compositions with an oxygen- containing gas.
- Useful catalyst compositions comprise a crystalline aluminosilicate or ferrosilicate, which is, optionally, combined with one, two, or more additional metals or metal compounds.
- Preferred combinations include:
- a crystalline aluminosilicate such as ZSM-5 or Zeolite L
- a Group 10 metal such as Pt
- a Group 1 alkali metal such as sodium or potassium
- a crystalline aluminosilicate such as ZSM-5 or Zeolite L
- a Group 10 metal such as Pt
- a Group 1 alkali metal such as sodium or potassium
- a crystalline aluminosilicate such as a ferrosilicate or an iron treated ZSM-5 combined with a Group 10 metal (such as Pt), a Group 1 alkali metal (such as sodium or potassium);
- a crystalline aluminosilicate (Zeolite L) combined with a Group 10 metal (such as Pt) and a Group 1 alkali metal (such as potassium); and
- a crystalline aluminosilicate such as ZSM-5 combined with a Group 10 metal (such as Pt), a Group 1 alkali metal (such as sodium), and a Group 11 metal (such as silver or copper).
- Another useful catalyst composition is a group 10 metal (such as Ni, Pd, and Pt, preferably Pt) supported on silica (e.g., silicon dioxide) modified by a Group 1 alkali metal silicate (such as Li, Na, K, Rb, and/or Cs silicates) and/or a Group 2 alkaline earth metal silicate (such as Mg, Ca, Sr, and/or Ba silicates), preferably potassium silicate, sodium silicate, calcium silicate and/or magnesium silicate, preferably potassium silicate and/or sodium silicate.
- a Group 1 alkali metal silicate such as Li, Na, K, Rb, and/or Cs silicates
- a Group 2 alkaline earth metal silicate such as Mg, Ca, Sr, and/or Ba silicates
- potassium silicate, sodium silicate, calcium silicate and/or magnesium silicate preferably potassium silicate and/or sodium silicate.
- the Group 10 metal content of the catalyst composition is at least 0.005 wt%, based on the weight of the catalyst composition, preferably, in the range from about 0.005 wt% to about 10 wt%, or from about 0.005 wt% up to about 1.5 wt%, based on the weight of the catalyst composition.
- the silica (Si02) may be any silica typically used as catalyst support such as those marketed under the tradenames of DAVISIL 646 (Sigma Aldrich), DAVISON 952, DAVISON 948 or DAVISON 955 (Davison Chemical Division of W.R. Grace and Company).
- the first reactor hydrocarbon effluent is cooled down once it exits the first reactor.
- the first reactor hydrocarbon effluent may be passed through at least one heat exchanger located next to the outlet from the first reactor where its temperature is lowered to a range from Tcl°C to Tc2°C, where Tel and Tc2 can be, independently, 20, 50, 80, 150, 200, 250, 300, 350, 400, or 450°C, as long as Tel ⁇ Tc2.
- the first reactor hydrocarbon effluent may be contacted with a quench liquid so that the temperature is lowered to a range from Tcl°C to Tc2 °C, where Tel and Tc2 can be, independently, 20, 40, 50, 60, 80, 100, 120, 140, 150, 160, 180, 200, 220, 240, 250, 260, 280, 300, 320, 340, 350, 360, 380, 400, 420, 440, or 450, as long as Tel ⁇ Tc2.
- Tel and Tc2 can be, independently, 20, 40, 50, 60, 80, 100, 120, 140, 150, 160, 180, 200, 220, 240, 250, 260, 280, 300, 320, 340, 350, 360, 380, 400, 420, 440, or 450, as long as Tel ⁇ Tc2.
- the first reactor hydrocarbon effluent comprises non-negligible amounts of heavy components, including but not limited to: polynuclear aromatic species (naphthalene and alkylated naphthalenes, anthracene and alkylated anthracenes, phenanthrene and alkylated phenanthrenes), DCPD, products formed as a result of undesired Diels-Alder reactions between CPD and acyclic diolefins. It is highly desired that these heavy components, especially C8+ hydrocarbons, are at least partly removed from the first reactor hydrocarbon effluent such that contamination of the C5-rich fraction and subsequent contamination of DCPD fractions by them are avoided.
- heavy components including but not limited to: polynuclear aromatic species (naphthalene and alkylated naphthalenes, anthracene and alkylated anthracenes, phenanthrene and alkylated phenanthrenes), DCPD, products formed as a
- naphthalene is very difficult to be removed from DCPD by distillation; also naphthalene and heavier PNAs can condense to form solids which can foul equipment. Therefore, naphthalene and heavier PNAs are desirably removed from the first reactor hydrocarbon effluent before it is further processed.
- such heavy components can be effectively removed in a vessel by contacting the stream of the first reactor hydrocarbon effluent, preferably after it is being partially cooled down, with a wash oil.
- the wash oil desirably in liquid phase during operation, can be sprayed into the washing vessel as liquid droplets when contacting the substantially vapor stream of the first reactor hydrocarbon effluent.
- the substantially vapor stream of the first reactor hydrocarbon effluent can be sent to a suitable gas-liquid contacting washing vessel capable of handling fouling services (e.g., a tower with grids and/or random packing).
- Sufficient contact between the first reactor hydrocarbon effluent and the liquid wash oil results in the extraction of the heavy components (i.e., C8+ hydrocarbons) from the substantially vapor stream of the first reactor hydrocarbon effluent into the wash oil liquid.
- a small amount of the wash oil may be entrained in the first reactor hydrocarbon effluent vapor stream at a low vapor pressure. The entrained wash oil can be removed subsequently where necessary.
- the first reactor hydrocarbon effluent vapor stream can be quenched down further to a temperature in a range from 10 to 300°C, preferably from 20 to 100°C.
- a vapor stream of the first reactor hydrocarbon effluent, washed and cooled is obtained.
- a wash oil liquid stream comprising multiple-ring aromatics mentioned above, may also be obtained.
- wash oils can be used.
- the wash oil include: cyclohexane; monoalkyl, dialkyl, and trialkyl cyclohexanes; benzene; monoalkyl, dialkyl, and trialkyl benzenes; monoalkyl, dialkyl, trialkyl, and tetraalkyl naphthalenes; other alkylated multiple-ring aromatics; and mixtures and combinations thereof.
- Preferred wash oils are: alkyl benzenes and mixtures thereof (herein referred to as light wash oil); and alkyl naphthalenes and mixtures thereof (herein referred to as heavy wash oil).
- toluene especially relatively pure toluene with a purity of at least 50 wt%, or alkylnaphthalene(s), especially those with purity of at least 50 wt%, is used as the wash oil.
- dimerization between CPD molecules may occur to form DCPD, and CPD may react with acyclic diolefins to form other C10+ hydrocarbons.
- a major portion of these heavy components, if formed, are partitioned in the wash oil liquid stream exiting the washing vessel.
- wash oil liquid stream is sent to a fuel disposition or other low value disposition directly, a portion of the CPD produced in the first reactor would be downgraded to low value.
- the upper C5-rich stream may be fed directly or indirectly to a second reactor as part of the first C5-rich fraction.
- the lower wash oil-rich stream can be further distilled to recover at least a portion of the wash oil, which can be recycled to the wash vessel directly or indirectly.
- Such conditions favoring reverse dimerization include, e.g., a temperature in the range from 150 to 350°C, preferably, from 170 to 260°C, a pressure in a range from 21 to 345 kilopascal absolute, preferably from 21 to 138 kilopascal absolute, and a residence time from 0.01 to 10 hours, preferably from 0.1 to 4 hours.
- the first reactor hydrocarbon effluent which is preferably cooled at the outlet of the first reactor as described above, and washed in a washing vessel as described above is then supplied via a fluid communication channel to a first separation sub-system and processed in the first separation sub-system to obtain a C5-rich fraction that is depleted of C1-C4 hydrocarbons and hydrogen, and desirably, depleted of heavy components such as C8+ hydrocarbons. Due to the nature of the reactions taking place in the first reactor, substantial volume of hydrogen is present in the first reactor hydrocarbon effluent.
- a compression train with inter-stage cooling and liquid/vapor separation can be advantageously used as the first separation sub-system to minimize the loss of C5 hydrocarbons to the hydrogen and light hydrocarbon stream.
- Exemplary compression trains with inter-stage cooling and liquid/vapor separation are those comprising at least 3-stages of compression/inter-stage cooling with an exiting pressure from the last stage of at least 100 psia (689 kilopascal absolute).
- first C5-rich hydrocarbon (the first C5-rich fraction) may be obtained from the multiple stages. Where multiple streams of the first C5-rich fractions are obtained, two or more of them may be, optionally, combined into a single first C5-rich rich fraction stream and then processed together subsequently.
- the first C5-rich fraction generally comprises: (i) CPD; (ii) unreacted C5 hydrocarbon(s) from the C5 feedstock such as n-pentane; and (iii) cyclopentane and cyclopentene.
- the first C5-rich fraction may further comprise a portion of the wash oil, especially if the wash oil contains C6 and C7 hydrocarbons, such as cyclohexane and alkylcyclohexanes, benzene and alkylbenzenes (e.g., toluene). Such wash oil may be removed subsequently where necessary. Even if high boiling point wash oils such as alkyl naphthalenes are used, the first C5-rich fraction may comprise C6 hydrocarbons (as byproducts from the first reactor) such as benzene at a low concentration.
- C6 and C7 hydrocarbons such as cyclohexane and alkylcyclohexanes, benzene and alkylbenzenes (e.g., toluene).
- the first C5-rich fraction may comprise C6 hydrocarbons (as byproducts from the first reactor) such as benzene at a low concentration.
- an optional heavy-containing stream may be produced, especially at one of the early stages, comprising wash oil and C8+ hydrocarbons (DCPD, and other products as a result of the Diels-Alder reactions between CPD and other dienes, e.g.), and the like.
- Such heavy stream can be in non-negligible quantity if high boiling point wash oil such as methylnaphthalene(s) is used. If such heavy stream is produced from the compression train, it may be advantageously combined with the wash oil liquid stream produced from the washing vessel described above, and then processed together subsequently.
- a light components-rich fraction comprising hydrogen and C1-C4 hydrocarbons is also obtained.
- This light components-rich fraction is desirably depleted of C5 components, especially CPD, or at least minimized, such that C5 molecules are used to the highest degree in the process of the present invention.
- a significant component of the light components-rich fraction coming from the first separation sub-system separating the first reactor hydrocarbon effluent is hydrogen gas.
- C1-C4 hydrocarbons are produced at small quantities in the first reactor from the C5 feedstock.
- a C1-C4 light hydrocarbon such as CH4 may be supplied to the first reactor as a co-feedstock, resulting in higher concentrations of the C1-C4 light hydrocarbons in the light components- rich fraction obtained from the first separation sub-system.
- PSA pressure-swing adsorption
- RCPSA rapid cycle pressure-swing adsorption
- TSA thermal-swing adsorption
- cryogenic processes membrane separation, and the like, with PSA or RCPSA being preferred.
- a hydrogen-rich stream comprising hydrogen at a purity of at least 95 mol%, based on the total moles of the hydrogen-rich stream; a middle stream comprising hydrogen and C1-C4 hydrocarbons that is preferably low in C2+ hydrocarbons; and a Cl-C4-rich hydrocarbon stream which may also contain C5+ hydrocarbons which can be subsequently recovered by washing or low temperature fractionation (absorber, e.g.).
- a portion of the hydrogen-rich stream and/or a portion of the middle stream (if C1-C4 hydrocarbon is co-fed into the first reactor) can be recycled to the first reactor.
- the middle stream and/or the C1-C4 hydrocarbon stream can be used as fuel gas to produce the thermal energy needed for certain steps (such as the conversion process in the first reactor) in the process of the present invention.
- the Cl-C4-rich hydrocarbon stream can be utilized as a feedstock for other process such as light olefins production and/or further processed to obtain an LPG fraction.
- the recycle hydrogen may be advantageously admixed with at least a portion of the C5 feedstock before being fed into the first reactor to reduce coke formation on the catalyst particles, thereby increasing the life of the catalyst used in the first reactor. Additionally or alternatively, the recycle hydrogen may be fed separately into the first reactor. Additionally or alternatively, the recycle hydrogen may be utilized for rejuvenation or reduction of the catalyst.
- the first C5-rich fraction advantageously comprises CPD at a high concentration in a range from cal wt% to ca2 wt%, based on the total weight of C5 hydrocarbons in the first C5-rich fraction, where cal and ca2 can be, independently, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, or 90, as long as cal ⁇ ca2.
- Such CPD may be used directly as a CPD feed for the production of, e.g., norbornene, vinyl norbornene, ethylidene norbornene, hydrocarbon resin adhesives or tackifiers, unsaturated polyester resins, cyclopentane, and/or cyclopentene.
- At least a portion of the first C5-rich fraction can be supplied to a first dimerization reactor (the second reactor in the system) operating under a first set of dimerization conditions, where a portion of the CPD is advantageously converted into DCPD.
- a first dimerization reactor the second reactor in the system
- This can be highly desirable because DCPD is much more stable than CPD, and therefore can be stored and/or transported to a different location where it is used as DCPD or converted into CPD and used for the production of value-added products.
- the first dimerization reactor (the second reactor in the system) can be advantageously a plug flow reactor, a back mixed reactor, a continuous stirred-tank reactor, a boiling point reactor, and/or a baffled reactor; additionally the reactor may contain heat transfer devices such as coils.
- the first dimerization reactor may consist of one or more reaction zones within a single vessel or in multiple vessels and may include one or more heat exchanging devices within the reaction zones or between the reaction zones.
- the first set of dimerization conditions in the first dimerization reactor can advantageously include: a temperature in the range from Tbl°C to Tb2°C, where Tbl and Tb2 can be, independently, 30, 50, 60, 80, 100, 120, 140, 150, 160, 180, 200, 220, 240, or 250, as long as Tbl ⁇ Tb2; an absolute pressure in the range from Pbl kilopascal to Pb2 kilopascal, where Pbl and Pb2 can be, independently, 345, 350, 400, 450, 500, 550, 600, 700, 800, 900, 1000, 1500, 2000, 2500, 3000, 3500, 4000, 4500, 5000, 6000, 6500, 6894, or 7000, as long as Pbl ⁇ Pb2; and a residence time in the range from Trl minutes to Tr2 minutes, where Trl and Tr2 can be, independently, 1, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100
- the first set of dimerization conditions include a temperature in the range from 70 to 130°C, a total pressure in the range from 689 to 3447 kilopascal absolute, and a residence time in the range from 20 to 200 minutes, such as from 100 to 200 minutes; preferably, if three dimerization reactors in series are utilized in the system, the first set of dimerization conditions include a temperature in the range from 90 to 140°C, a total pressure in the range from 689 to 3447 kilopascal absolute, and a residence time in the range from 1 to 30 minutes. [00118] A portion of the CPD contained in the first C5-rich fraction supplied into the first dimerization reactor is converted into DCPD.
- a second reactor effluent comprising CPD and DCPD.
- the degree of conversion in the second reactor is limited so that high purity DCPD may be produced; i.e., the extent of conversion is limited so that the quantity of CPD co- dimers with acyclic dienes and mono olefins is maintained below a level so as to be able to obtain the desired purity of DCPD.
- the first C5-rich fraction comprises CPD at a concentration of C(CPD)2 wt%, based on the total weight of C5 components in the first C5-rich fraction;
- the second reactor effluent comprises CPD at a concentration of C(CPD)3 wt% and DCPD at a concentration of C(DCPD)1, both based on the total weight of C5 hydrocarbons and CIO hydrocarbons in the second reactor effluent; and C(CPD)3 ⁇ C(CPD)2.
- At least a portion of the second reactor effluent is then supplied to a second separation device, such as a distillation column, where a first DCPD-rich fraction (as a lower stream such as a bottom effluent from the column, e.g.) and a second C5-rich fraction (as an upper stream such as an overhead effluent from the column, e.g.) are obtained.
- a first DCPD-rich fraction as a lower stream such as a bottom effluent from the column, e.g.
- a second C5-rich fraction as an upper stream such as an overhead effluent from the column, e.g.
- the first DCPD-rich fraction can have a DCPD concentration of C(DCPD)1 wt%; and xl ⁇ C(DCPD)1 ⁇ x2, wherein xl and x2 can be, independently, 80, 82, 84, 85, 86, 88, 90, 91, 92, 93 , 94, 95, 96, 97, 98, 99, 99.2, 99.4, 99.5, 99.6, 99.8, or 100, as long as xl ⁇ x2.
- Ultra high purity DCPD i.e., UHP DCPD
- UHP DCPD Ultra high purity DCPD with a concentration of at least 98 wt%, 99 wt%, or even 99.5 wt%, can be obtained as the first DCPD-rich fraction.
- At least a portion of the first DCPD-rich fraction can be, optionally, supplied to at least another separation device, such as a distillation column, where the purity of the first DCPD-rich fraction can be further increased.
- CPD concentration in the second C5-rich fraction tends to be lower than in the first C5-rich fraction.
- the second C5-rich fraction comprises CPD at a concentration in a range of from 95.0 wt% to 99.9 wt% based on the total weight of the second C5-rich fraction.
- At least a portion of the second C5-rich fraction obtained from the second separation device may advantageously comprise CPD at a high concentration in the range from ca3 wt% to ca4 wt%, based on the total weight of C5 hydrocarbons in the second C5- rich fraction, where ca3 and ca4 can be, independently, 1, 5, 10, 20, 25, 30, 35, 40, 45, 50, 55, or 60, as long as ca3 ⁇ ca4.
- Such CPD in the second C5-rich fraction may be directly used as a CPD feed for the production of, e.g., norbornene, vinyl norbornene, ethylidene norbornene, hydrocarbon resin adhesives or tackifiers, unsaturated polyester resins, cyclopentane, and/or cyclopentene.
- the second C5-rich fraction can be supplied to a second dimerization reactor (the third reactor in the system) operating under a second set of dimerization conditions, where a portion of the CPD is advantageously converted into DCPD, similar to the operation in the first dimerization reactor (the second reactor in the system), but preferably operating at a higher temperature and/or longer residence time to enable satisfactory conversion of the lower concentration CPD.
- the second set of dimerization conditions in the second dimerization reactor can advantageously include: a temperature in the range from Tb3°C to Tb4°C, where Tb3 and Tb4 can be, independently, 30, 50, 60, 80, 100, 120, 140, 150, 160, 180, 200, 220, 240, or 250, as long as Tb3 ⁇ Tb4; an absolute pressure in the range from Pb3 kilopascal to Pb4 kilopascal, where Pb3 and Pb4 can be, independently, 345, 350, 400, 450, 500, 550, 600, 700, 800, 900, 1000, 1500, 2000, 2500, 3000, 3500, 4000, 4500, 5000, 6000, 6500, 6894, or 7000, as long as Pb3 ⁇ Pb4; and a residence time in the range from Tr3 minutes to Tr4 minutes, where Tr3 and Tr4 can be, independently, 1, 10, 20, 30, 40, 50, 60, 70, 80, 90
- the second set of dimerization conditions include a temperature in the range from 75 to 140°C, such as from 100 to 140°C, a total pressure in the range from 689 to 3447 kilopascal absolute, and a residence time in the range from 100 to 300 minutes, such as from 150 to 300 minutes; preferably, if three dimerization reactors in series are utilized in the system, the second set of dimerization conditions include a temperature in the range from 100 to 140°C, a total pressure in the range from 689 to 3447 kilopascal absolute, and a residence time in the range from 1 to 30 minutes.
- the second dimerization reactor (the third reactor in the system) can be a reactor similar to the first dimerization reactor (the second reactor in the system).
- a portion of the CPD contained in the second C5-rich fraction supplied into the second dimerization reactor is converted into DCPD.
- a third reactor effluent is obtained comprising CPD and DCPD.
- the degree of conversion in the third reactor is limited so that high purity DCPD may be produced; i.e., the extent of conversion is limited so that the quantity of CPD co-dimers with acyclic dienes and mono olefins is maintained below a level so as to be able to obtain the desired purity of DCPD.
- At least a portion of the third reactor effluent can then be supplied to a third separation device, such as a distillation column, where a second DCPD-rich fraction (as a lower stream such as a bottom effluent from the column, e.g.) and a third C5-rich fraction (as an upper stream such as an overhead effluent from the column, e.g.) are obtained.
- a third separation device such as a distillation column
- the second DCPD-rich fraction can have a DCPD concentration of C(DCPD)2 wt%; and x3 ⁇ C(DCPD)2 ⁇ x4, wherein x3 and x4 can be, independently, 40, 50, 60, 65, 70, 75, 80, 82, 84, 85, 86, 88, 90, 91, 92, 93, 94, 95, 96, 97, 98, or 99 as long as x3 ⁇ x4.
- the purity of the second DCPD-rich fraction is lower than the first DCPD-rich fraction because of the lower ratio of CPD to acyclic diolefins in the second C5-rich fraction than the first C5-rich fraction.
- very high purity DCPD with a concentration of at least 90 wt%, or 92 wt%, or 93 wt%, or even 95 wt% can be obtained as the second DCPD-rich fraction.
- At least a portion of the second DCPD-rich fraction can be, optionally, supplied to at least another separation device, such as a distillation column, where the purity of the second DCPD-rich fraction can be further increased.
- CPD concentration in the third C5-rich fraction tends to be lower than in the second C5-rich fraction.
- the third C5-rich fraction comprises CPD at a concentration in a range of from 90.0 wt% to 99.5 wt% based on the total weight of the third C5-rich fraction.
- At least a portion of the third C5-rich fraction obtained from the third separation device may advantageously comprise CPD at a concentration in the range from ca5 wt% to ca6 wt%, based on the total weight of the C5 hydrocarbons in the third C5-rich fraction, where ca5 and ca6 can be, independently, 1, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, or 60, as long as ca5 ⁇ ca6.
- Such CPD in the third C5-rich fraction may be directly used as a CPD feed for the production of, e.g., norbornene, vinyl norbornene, ethylidene norbornene, hydrocarbon resin adhesives or tackifiers, unsaturated polyester resins, cyclopentane, and/or cyclopentene.
- the third C5-rich fraction can be supplied to a third dimerization reactor (the fourth reactor in the system) operating under a third set of dimerization conditions, where a portion of the CPD is advantageously converted into DCPD, similar to the operation in the first dimerization reactor (the second reactor in the system).
- the third dimerization reactor (the fourth reactor in the system) can be a reactor similar to the first dimerization reactor (the second reactor in the system), but preferably operating at a higher temperature and/or longer residence time to enable satisfactory conversion of the lower concentration CPD.
- a majority of the CPD contained in the third C5-rich fraction supplied into the third dimerization reactor is converted into DCPD.
- acyclic C5 diolefins e.g., 1,3-pentadiene; 1,4-pentadiene, 1,2-pentadiene, and/or 2-methyl-l,3-butadiene
- additional streams containing acyclic C5 diolefins e.g., steam cracked naphtha, light cat naphtha, heavy cat naphtha
- C6 diolefins e.g., methyl cyclopentadiene and hexadienes
- trimers and tetramers of the C5 and C6 species may also be advantageously produced.
- a fourth reactor effluent is obtained comprising CPD and DCPD, preferably in combination with other C5 co- dimers, -trimers, and/or -tetramers.
- the third set of dimerization conditions in the third dimerization reactor can advantageously include: a temperature in the range from Tb5 °C to Tb6 °C, where Tb5 and Tb6 can be, independently, 30, 50, 60, 80, 100, 120, 140, 150, 160, 180, 200, 220, 240, or 250, as long as Tb5 ⁇ Tb6; an absolute pressure in the range from Pb5 kilopascal to Pb6 kilopascal, where Pb5 and Pb6 can be, independently, 345, 350, 400, 450, 500, 550, 600, 700, 800, 900, 1000, 1500, 2000, 2500, 3000, 3500, 4000, 4500, 5000, 6000, 6500, 6894, or 7000, as long as Pb5 ⁇ Pb6; and a residence time in the range from Tr5 minutes to Tr6 minutes, where Tr5 and Tr6 can be, independently, 100, 200, 300, 400, 500, 600, 700
- the third set of dimerization conditions include a temperature in the range from 80 to 150°C, such as from 100 to 150°C, a total pressure in the range from 689 to 3447 kilopascal absolute, and a residence time in the range from 150 to 300 minutes.
- At least a portion of the fourth reactor effluent can then be supplied to a fourth separation device, such as a distillation column, where a third DCPD-rich fraction (as a bottom effluent from the column, e.g.) and fourth C5-rich fraction (as an overhead effluent from the column, e.g.) are obtained.
- a fourth separation device such as a distillation column
- the third DCPD-rich fraction can have a DCPD concentration of C(DCPD)3 wt%; and x5 ⁇ C(DCPD)3 ⁇ x6, wherein x5 and x6 can be, independently, 20, 30, 40, 45, 50, 55, 60, 65, 70, 75, 80, 82, 84, 85, 86, 88, 90, 91, 92, 93, 94, or 95, as long as x5 ⁇ x6.
- the purity of the third DCPD-rich fraction is lower than the second DCPD-rich fraction because of the lower ratio of CPD to acyclic dienes in the third C5-rich fraction than the second C5-rich fraction.
- moderate purity DCPD with a concentration of at least 70 wt%, 75 wt%, 80 wt%, 85 wt%, or 90 wt% can be obtained as the third DCPD-rich fraction.
- At least a portion of the third DCPD-rich fraction can be, optionally, supplied to at least another separation device, such as a distillation column, where the purity of the third DCPD-rich fraction can be further increased.
- CPD concentration in the fourth C5-rich fraction tends to be lower than in the third C5-rich fraction.
- At least a portion of the first, second, third, and fourth C5-rich fractions described above, if produced at all in the process of the present invention, can be recycled to the first reactor described above, where the unreacted C5 hydrocarbon(s) and partially converted C5 hydrocarbons from the C5 feedstock can be further converted into CPD.
- the first, second, third, and fourth C5-rich fractions may contain C6+ hydrocarbons, such as cyclohexane, benzene, toluene, and the like.
- C6+ hydrocarbons such as cyclohexane, benzene, toluene, and the like.
- a separation device such as a distillation column, to produce a fifth C5-rich stream and a C6+-rich stream.
- a purified fifth C5-rich fraction is then recycled to the first reactor.
- Mogas is a blended mixture comprising C4 through C12 hydrocarbons having an initial normal boiling point of about 35°C and a final boiling point of about 200°C. Mogas is used primarily as fuel for internal combustion engines in automotive vehicles. There are many different mogas specifications that have been mandated by various local, state, or national governmental agencies. One example is Reid Vapor Pressure (RVP) of final mogas product. The vapor pressure of mogas is a measure of its volatility and high vapor pressures resulting in high evaporative emissions of smog-forming hydrocarbons.
- RVP Reid Vapor Pressure
- Converting n-pentane to isopentane can result in a favorable increase in octane, but also an unfavorable increase in the RVP.
- Conversion of n-pentane to cyclopentyl and internal olefinic species - which occurs in the first reactor in the present invention - favorably increases the octane and favorably decreases the RVP.
- DCPD-rich streams may also be partially or fully hydrogenated to produce a low RVP / higher octane blend component.
- At least a portion of the first, second, third, fourth, and fifth C5-rich fractions and the C6+-rich stream described above, if produced at all in the process of the present invention, can be, optionally, combined with additional streams containing diolefins (e.g., steam cracked naphtha, light cat naphtha, heavy cat naphtha) and can be selectively hydrogenated to produce a mogas component.
- additional streams containing diolefins e.g., steam cracked naphtha, light cat naphtha, heavy cat naphtha
- first, second, third, fourth, and fifth C5-rich fractions contain high concentrations of unsaturated C5 hydrocarbons, including CPD and cyclopentene, once partially hydrogenated they tend to have higher octane-value and lower Reid Vapor Pressure (RVP) than the acyclic saturated C5 feedstock supplied to the first reactor.
- a "selective hydrogenation" process is a treatment of a mixture comprising both diolefins and mono olefins with hydrogen in the presence of a selective hydrogenation catalyst under selective hydrogenation conditions favoring the conversion of diolefins into mono olefins over the conversion of mono olefins into saturates.
- Such selective hydrogenation may be carried out in a hydrogenation reactor having a hydrogenation catalyst loaded therein.
- the selectively hydrogenated mogas component comprises diolefins at a total concentration not higher than 2.0 wt%, preferably not higher than 1.0 wt%, preferably not higher than 0.5 wt%, and ideally not higher than 0.1 wt% based on the total weight of the mogas component.
- This mogas component can then be blended with additional mogas components to obtain mogas with the desired composition and properties.
- At least a portion of the first, second, third, fourth, and fifth C5-rich fractions described above, if produced at all in the process of the present invention, and/or a portion of their hydrogenated products, may be separated to obtain high-purity cyclopentene, cyclopentane, 2-methyl-l,3- butadiene, and/or 1,3-pentadiene, each of which can be used or sold as valuable industrial materials.
- Non-limiting examples of hydrogenation catalyst include: palladium-based or nickel-based catalysts.
- Exemplary hydrogenation conditions include: a temperature in the range from 30 - 250°C and a pressure in the range from 1,700 - 5,500 kilopascal absolute.
- the present invention can be used to convert low value C5 feedstock into higher value CPD, DCPD, mogas components with high octane and/or lower RVP, cyclopentene, cyclopentane, 1,3-pentadiene, and the like, and hydrogen.
- FIG. 1 The drawings schematically illustrate the block flow diagrams of exemplary system(s) and sub-system(s) thereof of the present invention operating to implement exemplary process(es) or aspects thereof of the present invention. It should be understood that only major components are shown in the drawings. Auxiliary equipment such as control valves, pumps, heat exchangers, reboilers, recycle loop, and the like, although not all shown in all drawings, are used liberally throughout the whole process to manipulate stream and equipment thermodynamic conditions.
- a C5 feedstock stream 103 comprising n- pentane at, e.g., at least 50 wt% is combined with a hydrogen co-feedstock stream 105 to form a combined stream 107, which is then combined with a recycle third C5-rich stream 109 to form a combined feed stream 111, which is fed to a first reactor 113 (also labeled Rl).
- the molar ratio of hydrogen to the C5 feedstock in stream 111 can range from 0.1 to 3.0, preferably from 0.3 to 2.0, more preferably from 0.5 to 1.5.
- a major purpose of co-feeding hydrogen is to prevent coke formation on the catalyst, especially at locations where the in- situ produced hydrogen is at a relatively low concentration.
- the reactor 113 may be a fixed bed reactor with a bed of catalyst 115 loaded therein.
- the catalyst 115 is chosen from the compositions described above. Reactions of the C5 hydrocarbons in the presence of the catalyst particles are highly endothermic. Thus, reactor 113 is heated by external heating to maintain an internal temperature in the range from 450°C to 800°C.
- the weight hourly space velocity is in the range from 1 to 100 hour "1 .
- a substantial portion of the C5 hydrocarbons in the feed 111 is converted into CPD and byproducts such as acyclic diolefins, acyclic mono olefins, cyclopentane, cyclopentene; light components including hydrogen and C1-C4 hydrocarbons; one-ring aromatics; and multiple-ring aromatics at a total conversion of n- pentane in the range from 50% to 99%.
- a first reactor hydrocarbon effluent 117 is drawn at a temperature in the range from 500 to 800°C and at a total absolute pressure in the range from 20 to 700 kilopascal absolute.
- the first reactor hydrocarbon effluent 117 can comprise CPD at a total concentration in the range from 15 wt% to 80 wt%, on the basis of the total weight of C5 hydrocarbons in the first reactor hydrocarbon effluent 117.
- the first reactor hydrocarbon effluent stream 117 is promptly cooled down by one or more heat exchanger 119 to obtain a stream 121 to avoid undesired side reactions such as thermal cracking, condensation of PNAs, and premature Diels-Alder reactions of reactive diolefinic species, especially CPD.
- a quantity of wash oil (not shown) may be added prior to and/or within exchanger 119 to help prevent fouling.
- the cooled stream 121 and a wash oil steam 125 are then fed into a washing vessel 123, where the first reactor hydrocarbon effluent is also quenched down to obtain a washed first reactor hydrocarbon effluent stream 129.
- the wash oil used in the example shown in FIGs. 1 and 2 comprises alkylnaphthalene(s) and/or alkylbenzene at a total concentration of at least 50 wt%, although other wash oil as described above may be used.
- Stream 129 comprises C5 components and light components from the first reactor hydrocarbon effluent.
- Stream 129 may also contain C6, C7, C8, and the wash oil at non- negligible amounts.
- a wash oil bottom stream 127 comprising the wash oil, one-ring aromatics and multiple-ring aromatics, is also obtained from the washing vessel 123.
- the upper stream 129 as clean first reactor hydrocarbon effluent, is then supplied to a first separation sub-system 131 (also labeled SD1), where a first C5-rich stream 133, one or more additional C5-rich streams 134 (one shown in FIG. 1), and a light component stream 161 comprising hydrogen and C1-C4 hydrocarbons are obtained.
- the C5-rich streams 133 and 134 are advantageously depleted of C1-C4 hydrocarbons.
- Stream 133 can comprise one or more of C6, C7, C8+, and the heavy wash oil at non-negligible amounts.
- Stream 134 desirably comprises C6, C7, C8+, and the heavy wash oil at significantly lower concentrations than stream 133.
- stream 134 is essentially free of C10+ and the heavy wash oil.
- Stream 161 is fairly large in total volume, given the amount of hydrogen produced in the first reactor 113.
- stream 161 is further contacted with a wash oil stream 165 in vessel
- wash oil stream 163 (sometimes also called “debutanizer” or “debutanizer section”) to obtain a stream 167 comprising H 2 and C1-C4 hydrocarbons and depleted of C5 components.
- Stream 167 can be further separated by using various equipment and processes (now shown), such as PSA, RCPSA, TSA, cryogenic method, and membrane separation, to obtain one or more of the following: (i) a high-purity H2 stream; (ii) a H2/CI-C4 hydrocarbon mixture stream; and (iii) a Cl-C4-rich hydrocarbon stream.
- Stream 133 to the extent it may comprise one or more of C6, toluene, C8+, and the heavy wash oil at non-negligible concentration(s), is fed into a heavy wash oil (e.g., alkylnapthalene)-removal column 135 together with stream 127 described above, where an upper stream 137 rich in C5 and depleted of C10+, and a lower stream 138 comprising C7 and C8+ are obtained.
- Stream 138 may be purified in a subsequent distillation column (not shown) to obtain an alkylnapthalene-rich stream, which can be recycled to vessel 163 and/or washing vessel 123 described above.
- the conditions in the column 135 comprise advantageously a column bottom temperature in the range from 150 to 350°C, preferably from 170 to 260°C, and a total absolute pressure in the range from 3 psia to 50 psia (21 to 345 kilopascal absolute), preferably from 20 psia to 40 psia (138 to 276 kilopascal absolute), and a residence time in the range from 0.01 to 10 hours, preferably from 0.1 to 4 hours.
- Stream 137 and stream 134 both C5-rich and depleted of C10+, together as the first C5-rich fraction obtained from the first separation sub-system, is then delivered to the second reactor (also labeled R2, and called first dimerization reactor) 139 operating under a first set of dimerization conditions to convert a portion of the CPD contained therein into DCPD.
- the second reactor also labeled R2, and called first dimerization reactor
- the first set of dimerization conditions advantageously comprise: a temperature in the range from 30 to 250°C, preferably from 70 to 140°C, such as from 90 to 130°C, and a total absolute pressure in the range from 50 psia to 1000 psia (345 to 6895 kilopascal absolute), preferably from 100 psia to 500 psia (689 to 3447 kilopascal absolute), and a residence time in the range from 1 to 220 minutes, preferably from 20 to 200 minutes, such as from 100 to 200 minutes.
- Such conditions are optimized to favor the dimerization reaction between CPD molecules and to minimize the reactions between CPD and other diolefins.
- a second reactor effluent 141 comprising CPD, other C5 hydrocarbons, and DCPD is then fed into a second separation device 143 (SD2), which can be a distillation column.
- SD2 second separation device
- an ultra high-purity DCPD lower stream 147 and an upper stream comprising CPD and other C5 hydrocarbons are obtained.
- Stream 147 can comprise DCPD at a concentration of at least 95 wt%, such as 96 wt%, 98 wt%, 99 wt%, or even higher, based on the total weight of the CIO hydrocarbons of the stream 147.
- Stream 147 may be purified in a subsequent distillation column (not shown) to obtain (1) an ultra high-purity DCPD, which comprises DCPD at a concentration of at least 95 wt%, such as 96 wt%, 98 wt%, 99 wt%, or even higher, based on the total weight of the stream; (2) a light wash oil-rich stream, which can be recycled to vessel 163 and/or washing vessel 123 described above (not shown).
- an ultra high-purity DCPD which comprises DCPD at a concentration of at least 95 wt%, such as 96 wt%, 98 wt%, 99 wt%, or even higher, based on the total weight of the stream.
- a light wash oil-rich stream which can be recycled to vessel 163 and/or washing vessel 123 described above (not shown).
- the second set of dimerization conditions advantageously comprise: a temperature in the range from 30 to 250°C, preferably from 100 to 140°C, and a total absolute pressure in the range from 50 psia to 1000 psia (345 to 6895 kilopascal absolute), preferably from 100 psia to 500 psia (689 to 3447 kilopascal absolute), and a residence time in the range from 1 to 300 minutes, preferably from 150 to 300 minutes.
- a temperature in the range from 30 to 250°C, preferably from 100 to 140°C and a total absolute pressure in the range from 50 psia to 1000 psia (345 to 6895 kilopascal absolute), preferably from 100 psia to 500 psia (689 to 3447 kilopascal absolute), and a residence time in the range from 1 to 300 minutes, preferably from 150 to 300 minutes.
- Such conditions are optimized to maximize recovery of the remaining CPD while achieving on-spec production of a subsequent
- a third reactor effluent 151 comprising CPD, other C5 hydrocarbons, and DCPD is then fed into a third separation device 153 (SD3), which can be a distillation column.
- SD3 third separation device 153
- a high-purity DCPD lower stream 155 and an upper stream comprising CPD and other C5 hydrocarbons 157 are obtained.
- Stream 155 can comprise DCPD at a concentration of at least 90 wt%, such as 92 wt%, 94 wt%, 95 wt%, or even higher, based on the total weight of the CIO hydrocarbons of the stream 155.
- Stream 155 may be purified in a subsequent distillation column (not shown) to obtain (1) a high- purity DCPD, which comprises DCPD at a concentration of at least 90 wt%, such as 92 wt%, 94 wt%, 95 wt%, or even higher, based on the total weight of the stream; (2) a light wash oil- rich stream, which can be recycled to vessel 163 and/or washing vessel 123 described above (not shown).
- DCPD streams 147 and 155 may be sold or delivered as products. The user may convert these streams back into CPD or other compounds, depending on the intended applications.
- Upper stream 157 which is the third C5-rich fraction in the process of the present invention, can be fed into a third dimerization reactor (not shown), where the remaining CPD therein can be converted into an additional amount of DCPD, which can be separated and recovered as a third DCPD-rich fraction in a fourth separation device (not shown), if so desired.
- a third dimerization reactor is utilized, the preferred modes of operation for the first dimerization reactor and second dimerization reactor can be advantageously adjusted for the purpose of producing DCPD products at optimal quality levels, each with optimal quantities.
- the third DCPD-rich fraction would have a lower purity than the first and second DCPD-rich fractions produced upstream in the process as described above.
- the third C5-rich fraction stream 157 from the third separation device 153 is divided into two streams 159 and 161.
- stream 161 is then separated in distillation column 163 to obtain a fifth C5-rich stream 165 that is depleted with C6+ and a C6-rich stream 167.
- Stream 165 can then be recycled to the first reactor 113 (Rl) as stream 109, as described above.
- Stream 167 may be purged or used in other applications, such as an untreated mogas component as described below.
- Stream 159 (and, optionally, a portion of the first C5-rich fraction stream 137, and a portion of the second C5-rich fraction stream 145, not shown in FIG. 1) can be used for many purposes, due to the many useful components contained therein: CPD, cyclopentane, cyclopentene, pentene, pentadiene, 2-methylbutadiene, and the like.
- stream 159 (and other C5-rich fraction streams, and C6-rich stream 167) can be partly or entirely converted into a mogas component by selective hydrogenation to convert at least a portion of the dienes therein to mono olefins and/or saturates.
- the high concentrations of cyclopentane and cyclopentene in stream 159 after hydrogenation makes it particularly suitable for mogas blending due to the high octane and lower Reid Vapor Pressure values of cyclopentane and cyclopentene relative to the starting feedstock of acyclic C5 hydrocarbon such as n-pentane.
- the C6-rich stream 167 may be used directly as a mogas component after selective hydrogenation as well.
- stream 159 may be separated to obtain at least one pure stream of the following: cyclopentane, cyclopentene, pentene, 1,3-pentadiene, 1,4-pentadiene, and 2- methylbutadiene.
- FIG. 2 schematically illustrates an exemplary first separation sub-system 201 useful in the process and system of the present invention, particularly in the exemplary process illustrated in FIG. 1.
- the first separation sub-system 201 in FIG. 2 comprises a compression train including multiple-stage compression, cooling, and liquid/vapor separation.
- the upper stream 129 comprising a majority of cleaned first reactor effluent obtained from column 123 is first fed into a first-stage compressor 203, from which a stream 205 at a higher pressure is obtained.
- Stream 205 is then cooled by a first-stage heat exchanger 207 to obtain a liquid/vapor mixture stream 209, which is fed into a first-stage liquid/vapor separation device (such as a drum) 211 to obtain a first-stage lower liquid stream 215 comprising C5 hydrocarbons, but depleted of hydrogen and C1-C4 hydrocarbons and a first-stage upper vapor stream 213 comprising C5 hydrocarbons and rich in hydrogen and C1-C4 hydrocarbons.
- a first-stage liquid/vapor separation device such as a drum
- Stream 213 is then compressed by a second-stage compressor 217 to obtain a stream 219 with an even higher pressure, which is then cooled by a second-stage heat exchanger 221 to obtain a second-stage lower temperature liquid/vapor mixture stream 223, which is separated in a second-stage liquid/vapor separation device (such as a drum) 225 to obtain a second-stage lower liquid stream 229 comprising C5 hydrocarbons, but depleted of hydrogen and C1-C4 hydrocarbons and a second-stage vapor stream 227 comprising C5 hydrocarbons and rich in hydrogen and C1-C4 hydrocarbons.
- a second-stage compressor 217 to obtain a stream 219 with an even higher pressure
- a second-stage heat exchanger 221 to obtain a second-stage lower temperature liquid/vapor mixture stream 223, which is separated in a second-stage liquid/vapor separation device (such as a drum) 225 to obtain a second-stage lower liquid stream 229 comprising C5 hydrocarbons, but depleted of hydrogen and C1-
- Stream 227 is then compressed by a third-stage compressor 231 to obtain a stream 233 with an even higher pressure, which is then cooled by a third-stage heat exchanger 235 to obtain a lower temperature third-stage liquid/vapor mixture stream 237, which is separated in a third-stage liquid/vapor separation device (such as a drum) 239 to obtain a third-stage lower liquid stream 241 comprising C5 hydrocarbons, but depleted of hydrogen and C1-C4 hydrocarbons and a third-stage upper vapor stream 161 comprising rich in hydrogen and C1-C4 hydrocarbons and, optionally, comprising C5 hydrocarbons at a lower concentration.
- Stream 161 is then fed to a vessel 163 as illustrated in FIG. 1 and described above.
- stream 215 to the extent it may comprise non-negligible concentrations of at least one of the wash oil, C7, and C8+ (such as DCPD), can be fed into the heavy wash oil-removal column 135 together with stream 127, where it is processed to obtain a C5-rich stream 137 depleted with heavy wash oil as described above in connection with FIG. 1.
- Downstream streams 229 and 241 to the extent they tend to comprise lower concentrations of the heavy wash oil, C7, and C8+, may be combined to form a single stream 134, which is then combined with stream 137 as the first C5-rich fraction directly fed into the first dimerization reactor 139 (R2) as illustrated in FIG. 1.
- streams 215, 229, and 241 may be all delivered to the heavy wash oil-removal column 135 along with stream 127, where the C5-rich stream 137 is obtained and delivered to the first dimerization reactor 139.
- streams 215, 229, and 241 may be combined with stream 137 and then delivered directly to the first dimerization reactor 139.
- the first hydrocarbon reactor effluent obtained during the the acyclic Cs conversion process containing cyclic, branched and linear Cs hydrocarbons and, optionally, containing any combination of hydrogen, C4 and lighter byproducts, or Ce and heavier byproducts is a valuable product in and of itself.
- CPD and/or DCPD may be separated from the reactor effluent to obtain purified product streams, which are useful in the production of a variety of high value products.
- a purified product stream containing 50 wt% or greater, or preferably 60 wt% or greater of DCPD is useful for producing hydrocarbon resins, unsaturated polyester resins, and epoxy materials.
- a purified product stream containing 80 wt% or greater, or preferably 90 wt% or greater of CPD is useful for producing Diels-Alder reaction products formed in accordance with the following reaction Scheme (I):
- R is a heteroatom or substituted heteroatom, substituted or unsubstituted C1 -C50 hydrocarbyl radical (often a hydrocarbyl radical containing double bonds), an aromatic radical, or any combination thereof.
- substituted radicals or groups contain one or more elements from Groups 13-17, preferably from Groups 15 or 16, more preferably nitrogen, oxygen, or sulfur.
- a purified product stream containing 80 wt% or greater, or preferably 90 wt% or greater of CPD can be used to form Diels-Alder reaction products of CPD with one or more of the following: another CPD molecule, conjugated dienes, acetylenes, allenes, disubstituted olefins, trisubstituted olefins, cyclic olefins and substituted versions of the foregoing.
- Preferred Diels-Alder reaction products include norbornene, ethylidene norbornene, substituted norbomenes (including oxygen-containing norbornenes), norbornadienes, and tetracyclododecene, as illustrated in the following structures: d norbornene.
- the foregoing Diels-Alder reaction products are useful for producing polymers and copolymers of cyclic olefins copolymerized with olefins such as ethylene.
- the resulting cyclic olefin copolymer and cyclic olefin polymer products are useful in a variety of applications, e.g., packaging film.
- a purified product stream containing 99 wt% or greater of DCPD is useful for producing DCPD polymers using, for example, ring opening metathesis polymerization (ROMP) catalysts.
- the DCPD polymer products are useful in forming articles, particularly molded parts, e.g., wind turbine blades and automobile parts.
- Additional components may also be separated from the reactor effluent and used in the formation of high value products.
- separated cyclopentene is useful for producing poly cyclopentene, also known as polypentenamer, as depicted in Scheme (II).
- cyclopentane is useful as a blowing agent and as a solvent.
- Linear and branched Cs products are useful for conversion to higher olefins and alcohols.
- Cyclic and non-cyclic C5 products, optionally, after hydrogenation, are useful as octane enhancers and transportation fuel blend components.
- cyclopentane is useful as a blowing agent and as a solvent.
- Linear and branched C5 products are useful for conversion to higher olefins and alcohols.
- Cyclic and non-cyclic C5 products, optionally, after hydrogenation, are useful as octane enhancers and transportation fuel blend components.
- Examples 1-7 illustrate the invention. Examples 1-5 are obtained by using simulation. In these examples, the respective first reactor effluents are fed forward to the quench/wash section (123), a compression train section (SDl, 131), and a debutanization section (163) in similar manners as discussed above.
- All the recovered C5- rich fractions produced from the quench/wash section (135), the compression train section (SDl, 131), and debutanization section (163) are routed to the heavy wash oil removal column (135), and subsequently to a first dimerization reactor (R2, 139), an ultra high-purity DCPD recovery column (SD2, 143), a second dimerization reactor (R3, 149), and then a high-purity DCPD recovery column (SD3, 153).
- the process temperature, pressure, weight hourly space velocity, and molecular weight at the reactor inlet are 475°C, 62 psia (401.9 kilopascal absolute), 15 hr 1 , and 49.01 g/mol, respectively.
- Temperature and pressure at the reactor outlet are 575°C and 10 psia (68.9 kilopascal absolute), respectively.
- the reactions generate an additional 1.87 moles of molecules in the first reactor effluent exiting the outlet per mole of molecules in the total feed material at the inlet.
- This 1.87-fold molar expansion has the effects of lowering the molecular weight and density of the stream mixture from 49.01 g/mol at the inlet to 27.05 g/mol at the outlet and from 3.08 kg/m 3 at the inlet to 0.26 kg/m 3 at the outlet, respectively.
- the pressure drop from the inlet to the outlet of the first reactor is calculated to be about 52 psi (359 kilopascal). Composition of the first reactor effluent at the outlet is given in Table I below.
- a total weight of 308 tons of n-pentane feed is fed into the system (representing a CPD yield of 32.5 wt%, based on the total weight of the n-pentane feed), a total weight of 11.7 tons of hydrogen is produced, a total weight of 85 tons of UHP DCPD (stream 147) with purity level exceeding 99.0 wt% is produced, a total weight of 8 tons of DCPD (stream 155) with purity level exceeding 90.0 wt% is produced, and a total weight of 146 tons of mogas blend is produced.
- Example 2 (with 35% recycle of the third C5-rich fraction to the first reactor) requires 23.4% less of fresh n-pentane feed than Example 1 (without recycle of any of the C5-rich fraction to the first reactor).
- Example 2 produces 10.8% less of hydrogen than Example 1, due to using partially unsaturated feed vs. a fully saturated feed. This has the benefit of reduced volumetric flow rates in the reactor(s) and downstream equipment.
- the first reactor in Example 2 shows a 7.8% reduction in volumetric flow than in Example 1. This may have significant impacts on the equipment sizing of the downstream quench tower(s), gas compressor(s), and debutanizer(s).
- the enthalpy changes of the stream across the first reactor also shows significant reduction in Example 2 compared to Example 1. This translates into a 10.9 % reduction in furnace firing in Example 2, which can have a significant impact of the equipment sizing of the reactor(s) and fuel costs.
- the amount of heat required for sustaining the endothermic reactions in the first reactor is comparatively lower when using a partially converted C5 feedstock.
- Example 2 shows a 38.6 wt% of reduction of materials diverted to mogas production. Furthermore, it can be seen from Table I that the mogas stream in Example 2 has a slightly higher octane value of C5+ byproduct than in Example 1 since more kinetically limited isomerization and aromatization products will be concentrated into a smaller byproduct stream.
- Methylnaphthalene 0.00 0.000 0.00 0.00 - -
- the process temperature, pressure, weight hourly space velocity, and molecular weight at the reactor inlet are 475°C, 62 psia (401.9 kilopascal absolute), a lower weight hourly space velocity than Example 1 to attain a closer approach to thermodynamic equilibrium, and
- Example 1 Temperature and pressure at the reactor outlet are 575°C and 10 psia (68.9 kilopascal absolute), respectively.
- the reaction system also employs a different catalyst system from Example 1.
- the reactions generate an additional 2.02 moles of molecules in the first reactor effluent exiting the outlet per mole of molecules in the total feed material at the inlet.
- This 2.02-fold molar expansion has the effects of lowering the molecular weight and density of the stream mixture from 36.72 g/mol at the inlet to 18.16 g/mol at the outlet and from 2.44 kg/m 3 at the inlet to 0.18 kg/m 3 at the outlet, respectively.
- the pressure drop from the inlet to the outlet of the first reactor is calculated to be about 52 psi (359 kilopascal). Composition of the first reactor effluent at the outlet is given in Table III below.
- a total weight of 222 tons of n-pentane feed is fed to the system (representing a total CPD yield of 45.0 wt%, based on all weight of the n-pentane feed), a total weight of 18.3 tons of hydrogen is produced, a total weight of 54 tons of UHP DCPD with purity level exceeding 99.0 wt% (stream 147) is produced, a total weight of 44 tons of DCPD with purity level exceeding 90.0 wt% (stream 155) is produced, and a total weight of 77 tons of mogas blend is produced.
- a synthesis mixture with ⁇ 20.3% solids was prepared from 10,000 g of deionized (DI) water, 600 g of 50% NaOH solution, 25g of 45% Sodium Aluminate solution, 730 g of n-propyl amine 100% solution, 80 g of ZSM-5 seed crystals, and 3,190 g of Ultrasil PMTM. Modified silica were mixed in a 5-gal pail container and then charged into a 5-gal autoclave after mixing. The synthesis mixture had the following molar composition:
- the resulting ZSM-5 crystals had a S1O2/AI2O3 molar ratio of ⁇ 414, total surface area (SA)/(micropore SA + mesopore SA) of 490 (440 + 51) m 2 /g, Hexane sorption of 1 17 mg/g and an Alpha value (as measured on the proton form) of 31.
- a second portion of the material was used as synthesized for Pt impregnation.
- ZSM-5 having a S1O2/AI2O3 molar ratio of 414 and a sodium content of 0.38 wt% was calcined for 6 hours in nitrogen at 900°F (482°C). After cooling, the sample was reheated to 900°F (482°C) in nitrogen and held for three hours. The atmosphere was then gradually changed to 1.1 , 2.1, 4.2, and 8.4% oxygen in four stepwise increments. Each step was held for 30 minutes. The temperature was increased to 1000°F (540°C), the oxygen content was increased to 16.8%, and the material was held at 1000°F (540°C) for 6 hours.
- 0.5 wt% Pt was added via incipient wetness impregnation using an aqueous solution of tetraamine platinum hydroxide.
- the catalyst composition was dried in air at room temperature for 2 hours, then at 250°F (121 °C) for 4 hours, and lastly calcined in air at 660°F (349°C) for 3 hours.
- the catalyst composition powder was pressed (15 ton), crushed, and sieved to obtain 20-40 mesh particle size.
- Example 6 The above material of Example 6 was evaluated for performance.
- the catalyst composition (0.5 g) was physically mixed with quartz (1.5 g, 60-80 mesh) and loaded into a reactor.
- the catalyst composition was dried for 1 hour under He (100 mL/min, 30 psig (207 kPa), 250°C) then reduced for 1 hour under H 2 (200 mL/min, 30 psig (207 kPa), 500°C).
- the catalyst composition was then tested for performance with feed of n-pentane, H2, and balance He, typically at 550°C - 600°C, 5.0 psia (35 kPa-a) C5H12, 1.0 molar H 2 :C 5 Hi 2 , 14.7 h "1 WHSV, and 30 psig (207 kPa) total.
- Catalyst composition stability and regenerability was tested post initial tests at 550°C to 600°C by treatment with H 2 (200 mL/min, 30 psig (207 kPa), 650°C) for 5 hours, then retesting performance at 600°C.
- Table V and Table VI show the conversion of n-pentane and selectivity and yield of cyclic C5, CPD, iso-Cs, Ci, and C2-4 cracking products at varying temperatures (average values over 8 hours at each temperature) for a catalyst composition of 0.5 g ZSM-5(Si:Al2 molar ratio 414: l)/0.5wt%Pt at conditions of 5.0 psia (35 kPa-a) C5H12, 1 : 1 molar H2:Cs, 14.7 WHSV, 45 psia (310 kPa-a) total.
- the selectivities and yields are expressed on a molar percentage basis for the respective cyclic C5, CPD, iso-C5, CI, and C2-4 of hydrocarbons formed; i.e., the molar selectivity is the moles of the respective cyclic C5, CPD, Ci, and C2-4 formed divided by total moles of pentane converted.
- the selectivities and yields are expressed on a carbon percentage basis for the respective cyclic C5, CPD, iso-C5, CI, and C2-4 of hydrocarbons formed; i.e., the carbon selectivity is the moles carbon in the respective cyclic C5, CPD, iso-C5, CI, and C2-4 formed divided by total moles of carbon in the pentane converted.
- Table V and Table VI show greater than 80% conversion of pentane, at high WHSV, and 40% selectivity to cyclic C5 species at 595°C. While not the specific end product, cyclopentane and cyclopentene can be recycled to produce CPD.
- Tables VI and VIII further specify the individual iC5 components which are shown as totals in Tables V and VII.
- iC5o is iso pentane; including 2-methyl butane and 3- methyl butane.
- compositions, an element or a group of elements are preceded with the transitional phrase “comprising,” it is understood that we also contemplate the same composition or group of elements with transitional phrases “consisting essentially of,” “consisting of,” “selected from the group of consisting of,” or “is” preceding the recitation of the composition element, or elements and vice versa.
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WO2022138860A1 (en) * | 2020-12-24 | 2022-06-30 | Eneos株式会社 | Method for producing dicyclopentadiene |
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US2438400A (en) * | 1945-11-24 | 1948-03-23 | Sun Oil Co | Preparation of cyclopentadiene |
US2438401A (en) * | 1946-02-26 | 1948-03-23 | Sun Oil Co | Preparation of cyclopentadiene |
US2438404A (en) * | 1948-01-20 | 1948-03-23 | Sun Oil Co | Treatment of hydrocarbons |
DE2535809A1 (en) * | 1974-08-13 | 1976-03-04 | Shell Int Research | Cyclic 5C hydrocarbons from n-pentane feeds - by contact with hydrogen on a platinum-silica catalyst |
JPH0739354B2 (en) * | 1985-07-08 | 1995-05-01 | 日本ゼオン株式会社 | Method for producing high-purity dicyclopentadiene |
US4886926A (en) * | 1988-06-24 | 1989-12-12 | Mobil Oil Corporation | Catalytic dehydrogenation of hydrocarbons over tin-containing crystalline microporous materials |
DE3887990T2 (en) * | 1987-11-17 | 1994-06-01 | Mobil Oil Corp | DEHYDROGENATION CATALYST AND ITS USE. |
JPH03501942A (en) * | 1987-11-17 | 1991-05-09 | モービル オイル コーポレーシヨン | Dehydrogenation and dehydrocyclization catalysts, their synthesis and applications |
JP2001247490A (en) * | 2000-03-03 | 2001-09-11 | Nippon Petrochem Co Ltd | Method for producing dicyclopentadiene |
RU2186051C1 (en) * | 2000-10-30 | 2002-07-27 | Центр по разработке эластомеров Казанского государственного технологического университета | Method for production of dicyclopentadiene from c5 fraction of pyrolysis hydrocarbons |
CN1162380C (en) * | 2001-10-12 | 2004-08-18 | 中国石油化工股份有限公司 | Separation method of cracked C5 fraction |
US6958426B2 (en) * | 2001-09-29 | 2005-10-25 | China Petroleum & Chemical Corporation | Process for separating C5 cuts obtained from a petroleum cracking process |
CN100441554C (en) * | 2005-01-28 | 2008-12-10 | 中国石油化工股份有限公司 | Method of utilizing cracked, C5 fraction |
US7906568B2 (en) * | 2007-09-04 | 2011-03-15 | General Electric Company | Coupling agent composition and associated method |
CN101450886A (en) * | 2007-12-07 | 2009-06-10 | 中国石油化工股份有限公司 | Method for preparing dicyclopentadiene by carbon 5 fraction |
US20110178349A1 (en) * | 2010-01-20 | 2011-07-21 | Anzick Robert Kenneth | Method of treating a hydrocarbon stream comprising cyclopentadiene and one or more diolefins |
RU2463284C1 (en) * | 2011-05-04 | 2012-10-10 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Казанский национальный исследовательский технологический университет" | Method of producing dicyclopentadiene |
CN102951985A (en) * | 2011-08-17 | 2013-03-06 | 中国石油化工股份有限公司 | Method for separation of C5 fraction and preparation of cyclopentadiene |
US9248612B2 (en) * | 2011-12-15 | 2016-02-02 | General Electric Company | Containment case and method of manufacture |
EP2855167B1 (en) * | 2012-05-25 | 2017-03-22 | ExxonMobil Chemical Patents Inc. | Dicyclopentadiene based resin compositions and articles manufactured therefrom |
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