Boiling bed hydrogenation catalyst reactor online eddy flow method for activation recovering in situ and
Device
Technical field
This disclosure relates to a kind of boiling bed hydrogenation reactor, and in particular to a kind of boiling bed hydrogenation catalyst reactor is former
The online eddy flow method for activation recovering in position and device.
Background technique
Catalyst inactivation most important the reason is that: the sintering and isolation of (i) activity phase;(ii) catalyst duct and activity
Position is by the blocking of carbon distribution and metal deposit;(iii) poisoning of active sites.Catalyst duct and active sites are completely clogged with soot
Caused by inactivate, initially wrap up catalyst carbon distribution outer layer have permeability, mainly by with pre- graphitized carbon structure
Carbon distribution composition;As the cycle progresses, carbon distribution is continuously accumulated, and the permeability that catalyst carbon deposition outer layer spreads liquid is got over
It is poorer to come, and the activity and selectivity of catalyst is caused to reduce;Catalyst granules in fluidized bed reactor is by liquid and bubble
Continuous action and be shaken and wash, cause catalyst compared with fixed bed have the lower micro- charcoal amount of sticking (Roberto
Galiasso Tailleur, Lino Caprioli.Catalysis Today (catalysis today), 2005,109 (1-4): 185-
194), so that catalyst life has certain extension compared with the catalyst life in fixed bed.
Currently, the shape that industrialized boiling bed hydrogenation reactor technology can be fluidized according to catalyst in reactor both at home and abroad
State is divided into two kinds: (1) expanded bed state, i.e. gap between gas-liquid two-phase catalyst filling particle, so that catalyst bed is swollen
It is swollen to certain altitude, the interface of liquid-solid two-phase can be obviously observed on reaction bed top, with " H-Oil " and " LC-
Fining " technology and its deriving technology are representative;(2) another is complete mixing flow state, i.e., under the momentum transmitting of gas-liquid two-phase,
At the top of catalyst granules expansion reaction bed, there is no the interface of apparent liquid-solid two-phase, in reaction bed with middle petrochemical industry
" STRONG " technology is representative.
Under expanded bed state, control catalyst bed is expanded to certain altitude, for not above the catalyst bed of expansion
Gas-liquid mixture containing solid;In fact, the catalyst bed of this expanded bed state is a kind of dense state of catalyst, catalysis
Agent particle is in disordered state movement, and liquid phase must control in lesser extent the disturbance of catalyst, because disturbance is strong
The increase of degree increased dramatically the abrasion between the catalyst granules that will lead to dense state so that the size of catalyst granules and
Mechanical strength is continued to run without being able to satisfy boiling bed hydrogenation reactor by destroying.Alternatively, strength of turbulence is excessive to be caused to urge
Agent bed, which excessively expands, escapes out boiling bed hydrogenation reactor, so that entire boiling bed hydrogenation device is stopped work.Expanded bed state
Boiling bed hydrogenation reactor technology, either " H-Oil ", " LC-Fining " technology and its deriving technology, development are from the U.S.
Patent USRE.25,770;The subsequent United States Patent (USP) US 3,197,288 and US 4 for improving patent such as HRI company, 221,653,
The U.S. Patent application US 4 of 4,971,678, the Acomo company of United States Patent (USP) US 4,886,644 and US of Texaco company,
The United States Patent (USP) US 7,449,155 of 911,893 and US 4,950,459A, Shell company.United States Patent (USP) USRE.25,770 and
The fluidized state of its above-mentioned subsequent improvement patent, the reaction bed in disclosure is expanded bed state, needs to pass through control
System circulation oil stream amount, catalyst bed expansion height in active control fluidized bed reactor, catalyst bed expansion height with
The upper decanting zone for catalyst granules to obtain the gas-liquid two-phase for being free of solid particle, reactor head using circulation cup or
Circulation cup equipped with gas-liquid cyclone separator realizes that the gas-liquid separation of reactor head, the clear liquid-phase product of extraction are used as and follow
Ring oil or product.Since the separation for catalyst is realized by gravitational settling, the selection for catalyst system
Operation with reactor has specific requirement, and as follows: (1) catalyst size is larger, has preferable settling property, such as U.S.
It is " at least about 1/32 inch of average diameter that patent USRE.25,770 specification the 1st, which arranges the catalyst size suggested in the 66th row,
(i.e. 0.8mm), most common range are 1/16~1/4 inch (i.e. 1.6mm~6.35mm) ";Commercial plant is mostly diameter 1mm,
The bar rope shape catalyst granules of length 2mm;(2) active control catalyst bed expansion height, such as United States Patent (USP) USRE.25,770
Specification the 10th arrange and disclose that " the static bed is expanded to few 10%, and is no more than 50% in the claim 11 of the 18th row;
So that the catalyst granules can free movement in bed upon inflation, and do not take catalyst out of from catalyst bed ";The U.S.
Patent USRE.25,770 subsequent improvement patented technology still must although the expansion rate of catalyst bed can be improved
The expansion height that catalyst bed must be controlled, is no more than 100%, reserves the space of catalyst sedimentation.In brief, above-mentioned expansion
The catalyst system and operating condition of the fluidized bed reactor of bed state cannot always make gas-liquid two-phase for catalyst granules
Disturb excessive, therefore for the carbon distribution presoma on Removal of catalyst, the service life for extending catalyst is always extremely limited, Jin Jinhao
In catalyst solid particle in completely motionless fixed bed reactors.
The fluidized bed reactor of complete mixing flow state is the partial size by reducing catalyst granules, so that catalyst granules fluidizes
Required fluidizing velocity is lower compared with expanded bed state and realizes, catalyst can be fluidised to the charge level height of reactor, entirely
Reaction bed is all gas-liquid-solid three-phase mixture, therefore gas-liquid two-phase is smaller for the disturbance of catalyst.The boiling of complete mixing flow state
Bed hydroprocessing reactor technology is risen, using middle petrochemical industry " STRONG " technology as representative, representative patents are Chinese invention patent Shen for the country
It please CN1448212A;Its reactor head is provided with the three phase separator of three layers or multilayer concentric tube-in-tube structure form, passes through folding
The method of stream sedimentation realizes that catalyst is trapped in the purpose that interior reactor, reaction gas and liquid remove reactor;Therefore work as and urge
Agent completes gravitational settling operation in three phase separator, and catalyst granules completely cannot be disturbed only heavy with gravity
Reduction of speed degree.Then on the basis of Chinese invention patent application CN1448212A, Chinese invention patent application CN101376092 is public
Having opened in the three phase separator lower end of concentric tube-in-tube structure form setting cross sectional shape is trapezoidal or bowed guide frame, in
State application for a patent for invention CN101721961A discloses the increase diamond shape below the three phase separator of concentric tube-in-tube structure form and leads
Flow cone internals, Chinese invention patent application CN101618305 disclose one kind and changeover portion and expanding reach are arranged in reactor head,
Chinese invention patent application CN101721960A is inverted-cone shape and lower part by the way that concentric inner barrel and outer barrel is designed as top
It is positive and sets taper, the separation condition of Lai Youhua gravitational settling;Above-mentioned these hold Chinese invention patent application CN1448212A
It is continuous to improve, the technical thought of Chinese invention patent application CN1448212A is not still got rid of, is all that gas is implemented by inner cylinder
Abjection, then using the annular space channel between inner barrel and outer barrel and the annular space channel between outer cylinder and reactor shell to degassing
Catalyst pulp implements gravitational settling to realize the separation of catalyst and oil product.Chinese invention patent application CN101618305
Claim 1 disclosure 1.2~2 times of reactor direct tube section " diameter of expanding reach be ", i.e., it is straight using 2 times of direct tube sections
The expanding reach of diameter designs, and the area of section of baffling sedimentation obtained is 1.5 times of direct tube section, makes the liquid phase linear speed in expanding reach
Degree is reduced to the 66% of direct tube section liquid linear velocity, i.e., the particle and liquid velocity in three phase separator are smaller.Furthermore especially
It is worth noting that, in order to balance complete mixing flow state and sedimentation separation, general such boiling bed hydrogenation reactor is generally adopted
With the lesser catalyst of size, (the described in embodiment 1 of such as Chinese invention patent application CN1448212A uses 0.1~0.2
Millimeter microspherical catalyst) and lesser operation gas-liquid speed.The lesser catalyst granules of size has preferable fluidizing performance, often
Only just realize that complete mixing flow operates under the action of feedstock oil;But the interference of the lesser catalyst granules of size (or freely) heavy
Reduction of speed degree is also smaller;It needs to control the linear velocity of liquid in reactor in lower level, is just able to satisfy in three phase separator and uses
It is less than interference (or free) sinking speed of catalyst granules in the linear velocity of liquid in the annular space of baffling sedimentation, realizes separation;
101376092 B of Chinese invention patent CN 10172196 B and CN is also to continue Chinese invention patent application CN1448212A
Baffling settles thinking;107297186 B of Chinese invention patent CN is related to a kind of three phase separator structure, in Chinese invention patent
On the basis of 101376092 B of CN 10172196B and CN, the logistics in baffling sedimentation type three phase separator is separated into flow direction
Be changed to three-phase logistics and rise from the outermost layer channel of baffling sedimentation type three phase separator deaerate, two-phase logistics baffling after degassing into
Enter the gravitational settling under the middle layer progress bubble-free disturbed condition of baffling sedimentation type three phase separator, the liquid phase object of final clarification
Reactor is discharged in the central core that stream enters baffling sedimentation type three phase separator.108144555 A of Chinese invention patent application CN is related to
And a kind of three phase separator is provided with suction tube in reactor outlet, cooperation exists in the technical foundation of 107297186 B of CN
The eddy flow guide plate being arranged in the central core of baffling decanter type three phase separator, plays vacuum flashing and prevents liquid from being carried secretly by gas
Effect, solid particle is still to be separated by the gravitational settling of low velocity, can not implement big intensity to catalyst granules
Disturbance realize the removing of the carbon distribution presoma in catalyst particle surface and duct.
In 103769014 A of Chinese invention patent application CN 103773490 A and CN, three collected of reactor head
Phase reaction object passes through cyclone separator, but not only cannot achieve three phase separation but also cannot achieve the removing of catalyst, it is necessary to anti-
It answers device outlet to be provided in the high-pressure separator for being provided with multistage baffle of special designing further to be separated, catalyst is held
It is continuous to take reactor out of and accumulated in high-pressure separator, cause device to be unable to operate normally;Presence of the bubble in cyclone separator simultaneously,
Since the wake effect and sticking effect of bubble reduce rotational velocity of the catalyst granules in cyclone separator.
105363392 B of Chinese invention patent CN is being provided with a point fluidized bed reactor for chamber decanter type three phase separator
Liquid outlet after be provided with the surge tank of spinning liquid structure, with to due to dividing chamber decanter type three phase separator separating capacity insufficient
Caused catalyst entrainment implements secondary solid-liquor separation, but must cooperate the circulation swabbing action of circulation type fluidized bed reactor
It is just able to satisfy application under the collective effect of longer liquid leg effect, therefore such rotary filter press structure can be only installed at reaction
Outside device.The U.S. US 3,668,116 of Esso company can only also be provided with liquid phase rotation outside slurry bed system (ebullated bed) reactor device
Stream separator, the entrance of the cyclone separator are submerged in the charge level of reactor or less, position more than catalyst bed expansion height
It sets;Gaseous products in reactor directly go to recycle hydrogen system by the top discharge of reactor, and liquid-phase product is by external
The liquid phase of the separation of liquid phase cyclone separator, acquisition goes to high-pressure separator;External liquid phase cyclone separator is due to system stream
Journey is longer, and catalyst granules is lacking the extended stationary periods in hydrogen environment for a long time, makes the risk of the coking of catalyst more tight instead
It weighs.
In conclusion fluidized bed reactor both domestic and external is limited to fluidization operation and separation requirement in conversion zone at present,
Lower speed can only be maintained at.Gravitational settling hand is relied on mostly in the separated region of current fluidized bed reactor both domestic and external
Section, the movement velocity of catalyst granules are lower than conversion zone.Although it has been reported that the catalyst in fluidized bed reactor is disturbed
Movement with can slow down catalyst carbon deposition, extend catalyst life, but not yet see in engineering technology force regulation be catalyzed
Agent motion state come realize catalyst slow down catalyst carbon deposition, extend catalyst life method and apparatus.
Therefore, slow down there is an urgent need in the art to developing the realization catalyst for the defect that can overcome the above-mentioned prior art and urge
Agent carbon distribution, the method and apparatus for extending catalyst life.
Summary of the invention
Present disclose provides a kind of novel boiling bed hydrogenation catalyst reactor online eddy flow activation recovering sides in situ
Method and device, solve problems of the prior art.
The purpose of the present invention is realizing catalyst granules orderly rotation in the liquid phase and revolution motion condition regulation, reach
The purpose of carbon distribution presoma and initial carbon film on online Removal of catalyst particle in situ, so that catalyst granules coking process is big
Width slows down, the cycle of operation of boiling bed hydrogenation reactor substantially extends.
On the one hand, present disclose provides a kind of boiling bed hydrogenation catalyst reactor online eddy flow activation recovering sides in situ
Method, method includes the following steps:
(a) three-phase mixture being made of in boiling bed hydrogenation reactor gas phase, liquid phase and catalyst granules is in ebullated bed
Deaerate the two-phase mixture for obtaining gas phase and being made of liquid phase and catalyst granules in hydrogenator;
(b) resulting two-phase mixture is forced to make rotating motion to form eddy flow stream in the boiling bed hydrogenation reactor
, and regulate and control catalyst granules and revolve in the Swirling Flow around Swirling Flow central axis and around catalyst granules center
The coupled motions state of axis rotation;And
(c) centrifugal force that the revolution motion using catalyst granules in the Swirling Flow generates realizes catalyst granules
Separation from the two-phase mixture is trapped in boiling bed hydrogenation reactor, the clarification liquid phase without catalyst granules with
The boiling bed hydrogenation reactor is brought out as product after the obtained gas phase mixing that deaerates.
In one preferred embodiment, the three-phase mixture being made of gas phase, liquid phase and catalyst granules exists
Occupied height is exactly the liquid level in boiling bed hydrogenation reactor in the boiling bed hydrogenation reactor;In the liquid level
It is the gas-phase space that the gas phase to be deaerated by the three-phase mixture is formed above height.
In another preferred embodiment, in step (a), the catalyst granules is to have supported the periodic table of elements
In the poriness silicon oxide of alloy that is formed from IIIB race to Group IIB transition metal element and them or porous carbon or work
The bar rope shape particle of the metal oxide of carrier, particle diameter are 0.2~5mm, and draw ratio is 1~5;Alternatively, the catalysis
Agent particle is supported the alloy formed from IIIB race to Group IIB transition metal element and them in the periodic table of elements more
Permeability silica or porous carbon or make carrier metal oxide spheric granules, particle diameter be 0.2~5mm;It is described
The loadings of catalyst granules account for 20~85 volume % of the boiling bed hydrogenation reactor.
In another preferred embodiment, in step (b), by being built in boiling bed hydrogenation reactor head
The water conservancy diversion of impeller guide ring in catalyst eddy flow activation recovering device forces resulting two-phase mixture in the boiling bed hydrogenation
It makes rotating motion to form Swirling Flow in reactor, and regulates and controls catalyst granules in the Swirling Flow around Swirling Flow center
Axis revolution and the coupled motions state around catalyst granules central axis rotation.
On the other hand, present disclose provides a kind of boiling bed hydrogenation catalyst reactor online eddy flow activation recoverings in situ
Device, the device include:
Boiling bed hydrogenation reactor shell and the catalyst eddy flow activation recovering for being built in boiling bed hydrogenation reactor head
Device, wherein the catalyst eddy flow activation recovering device is by shell of column, the cone section connecting with shell of column, the impeller guide being placed in shell of column
Ring, the non-return guide cone connecting with catalyst recurrent canal, is placed in shell of column and stretches out column the catalyst recurrent canal connecting with cone section
The liquid phase overflow pipe of section and the gas-liquid connecting with reactor head mix outlet pipe composition;Wherein, the upper surface of the liquid phase overflow pipe
Higher than the liquid level in the boiling bed hydrogenation reactor.
In one preferred embodiment, be provided in the boiling bed hydrogenation reactor 1 or more it is in parallel
Catalyst eddy flow activation recovering device.
In another preferred embodiment, the impeller guide ring is made of multiple swirl vanes, the eddy flow leaf
Piece the shell of column standoff height be the shell of column height 5~20%, the inclination of the swirl vane relative level
Angle is 15~80 °, has fan-shaped overlapping region, and the central angle of the fan-shaped overlapping region between adjacent two pieces of swirl vanes
It is 1~10 °;The impeller guide ring is made of one or more helical ducts.
In another preferred embodiment, the upper end of the cone section connects the lower end of the shell of column, bores the lower end of section
Connect the upper end of the catalyst recurrent canal;Cone section is inverted conical, and axis is overlapped with the axis of the shell of column, bus
The angle in same level face is 5~89 °.
In another preferred embodiment, the boiling bed hydrogenation reactor shell is from bottom to top by coaxial lower part
Latus rectum section, middle part taper reducer and top expanding reach composition, the diameter of the top expanding reach be lower part latus rectum section 100~
200%, the height of top expanding reach is the 2~20% of lower part latus rectum section height;Middle part taper reducer is for connecting lower part
The inverted-cone shape of latus rectum section and top expanding reach, the angle in bus same level face are 30~60 °.
In another preferred embodiment, the boiling bed hydrogenation reactor be used for containing aerobic, sulphur, nitrogen, chlorine and
Hydrotreating, hydrofinishing and the hydrocracking process of the macromolecule hydrocarbon of metal impurities atom, hydroconversion condition are as follows: operation temperature
Degree is 250~500 DEG C, and operating pressure is 5~30MPa, and reaction weight hourly space velocity is 0.2~4h-1, hydrogen to oil volume ratio 200
~3000.
The utility model has the advantages that
The major advantage of methods and apparatus of the present invention is:
1) catalyst online eddy flow activation recovering operation in situ, the coking process of catalyst substantially slow down, the longevity of catalyst
Life substantially extends.
2) in catalyst online eddy flow activation recovering operating process in situ, the synchronous three-phase for realizing fluidized bed reactor outlet
Lock out operation, entire hydrogenation technique process short route.
Detailed description of the invention
Attached drawing is provided for a further understanding of the present invention, it simply forms a part of this specification with into one
Step explains the present invention, is not construed as limiting the invention.
Fig. 1 is that the boiling bed hydrogenation catalyst reactor eddy flow activity of a preferred embodiment according to the present invention is extensive
The structural schematic diagram of apparatus for coating.
Fig. 2 is that the boiling bed hydrogenation catalyst reactor eddy flow activity of a preferred embodiment according to the present invention is extensive
The structural schematic diagram of catalyst eddy flow activation recovering device in apparatus for coating.
Fig. 3 is tangential in combined vortex in the catalyst eddy flow activation recovering device of a preferred embodiment according to the present invention
VELOCITY DISTRIBUTION and catalyst granules are from, revolution motion schematic diagram.
Fig. 4 is the boiling bed hydrogenation catalyst reactor eddy flow activity of another preferred embodiment according to the present invention
The structural schematic diagram of recovery device.
Fig. 5 is according to the embodiment of the present application 1 using boiling bed hydrogenation catalyst reactor eddy flow activity of the invention
The process flow diagram of recovery device.
Fig. 6 is according to the embodiment of the present application 2 using boiling bed hydrogenation catalyst reactor eddy flow activity of the invention
The process flow diagram of recovery device.
Fig. 7 is according to the embodiment of the present application 3 using boiling bed hydrogenation catalyst reactor eddy flow activity of the invention
The process flow diagram of recovery device.
Specific embodiment
Present inventor by for a long time to the research of rotational flow field, find rotation of the particle in liquid phase eddy flow field,
Revolution and the certainly effect of revolution coupled oscillations, can effectively strengthen the reinforcing of liquid-solid micro-interface transmittance process;Meanwhile it being put forward for the first time
Boiling bed residual oil may be implemented and add at the de-oiling of hydrogen outlet catalyst using the particle rotation in cyclone and coupled motions of revolving
Reason realizes the removing on boiling bed residual oil Hydrogenation catalyst granule surface and the hydrocarbons in duct.Ebullated bed outlet is urged
" the Handbook of Spent that the offline deoiling treatment method of agent ex situ has been write by E.Furimsky et al.
Hydroprocessing Catalysts " (Second Edition) (useless hydrogen processing Catalyst Handbook (second edition)) included.
The characteristics of combined catalyst coking and deactivation process, i.e. heavy hydrocarbon, are attached on catalyst surface and duct is persistently condensed coking, first
It is initially formed soluble carbon distribution presoma, carbon distribution presoma is persistently condensed coking and forms the permeability for initially wrapping up catalyst
Carbon distribution outer layer, carbon distribution are continuously accumulated, and the permeability that catalyst carbon deposition outer layer spreads liquid worse and worse, causes catalyst
Activity and selectivity reduce.Therefore, as the eddy flow degreasing process of outlet catalyst granules, using in liquid phase cyclone
Soluble carbon distribution presoma in catalyst surface and duct and permeability are implemented in particle rotation and revolution coupled motions
The removing of initial carbon distribution, then the catalyst granules that coking and deactivation tendency may be implemented restores initial activity, i.e. catalyst
Activity is restored by eddy flow.However, it is foreseeable that if as previous catalyst deoiling treatment process outside reactor
Implement, inevitable process is very long;Catalyst stops for a long time in poor hydrogen hot environment, more increases catalyst coking and deactivation
Risk.Therefore for the optimum operation of the catalyst eddy flow activation recovering in the boiling bed hydrogenation reactor of high temperature and pressure be exactly
Reactor original position on-line implement, the catalyst retention that eddy flow activation restores participate in hydrogenation reaction in the reactor, and described is " former
Position " refers to that the operation is completed in the reactor locating for catalyst, and described " online " refers to that the operation adds in ebullated bed
It is completed in hydrogen reactor normal course of operation.Catalyst, liquid phase, gas phase three-phase are in the conversion zone of boiling bed hydrogenation reactor
How the state of mixed and disorderly disordered motion regulates and controls the disordered motion state that catalyst granules is detached from three-phase mixture of realizing, enters
Only orderly rotation and revolution motion state in the liquid phase is the key that realize catalyst eddy flow activation recovering.
The present invention realizes catalyst granules orderly rotation in the liquid phase and revolution motion condition regulation, has reached original position
The purpose of carbon distribution presoma and initial carbon film makes so that catalyst activity position exposes again on online Removal of catalyst particle
Catalyst granules coking process substantially slows down, the cycle of operation of boiling bed hydrogenation reactor substantially extends.By long-term heat
Mould and cold work die verifying, the present invention are accomplished.
In the disclosure in a first aspect, providing a kind of boiling bed hydrogenation catalyst reactor online eddy flow activity in situ
Restoration methods, method includes the following steps:
(a) three-phase mixture being made of in boiling bed hydrogenation reactor gas phase, liquid phase and catalyst granules is in ebullated bed
Deaerate the two-phase mixture for obtaining gas phase and being made of liquid phase and catalyst granules in hydrogenator;
(b) resulting two-phase mixture is forced to make rotating motion to form eddy flow stream in the boiling bed hydrogenation reactor
, and regulate and control catalyst granules and revolve in the Swirling Flow around Swirling Flow central axis and around catalyst granules center
The coupled motions state of axis rotation;And
(c) centrifugal force that the revolution motion using catalyst granules in the Swirling Flow generates realizes catalyst granules
Separation from the two-phase mixture is trapped in boiling bed hydrogenation reactor, the clarification liquid phase without catalyst granules with
The boiling bed hydrogenation reactor is brought out as product after the obtained gas phase mixing that deaerates.
In the disclosure, the three-phase mixture being made of gas phase, liquid phase and catalyst granules adds in the ebullated bed
Occupied height is exactly the liquid level in boiling bed hydrogenation reactor in hydrogen reactor;It is above the liquid level
The gas-phase space formed by the gas phase that the three-phase mixture deaerates.
In the disclosure, in step (a), the catalyst granules, which can be, have been supported in the periodic table of elements from IIIB race
The poriness silicon oxide or porous carbon of the alloy formed to Group IIB transition metal element and between them or the metal for making carrier
The bar rope shape particle of oxide, particle diameter can be 0.2~5mm, and draw ratio can be 1~5.
In the disclosure, the catalyst granules, which can be, has supported in the periodic table of elements from IIIB race to Group IIB transition
The poriness silicon oxide or porous carbon of metallic element and the alloy formed between them or make carrier metal oxide ball
Shape particle, particle diameter can be 0.2~5mm.
In the disclosure, the loadings of the catalyst granules account for 20~85 bodies of the boiling bed hydrogenation reactor
Product %.
In the disclosure, in step (b), by the catalyst eddy flow activity for being built in boiling bed hydrogenation reactor head
The resulting two-phase mixture of water conservancy diversion pressure of impeller guide ring in restorer is done in the boiling bed hydrogenation reactor to be rotated
Movement forms Swirling Flow, and regulates and controls catalyst granules and revolve in the Swirling Flow around Swirling Flow central axis and around catalysis
The coupled motions state of agent particle central axis rotation.
In the second aspect of the disclosure, a kind of boiling bed hydrogenation catalyst reactor online eddy flow activity in situ is provided
Recovery device, the device include:
Boiling bed hydrogenation reactor shell and the catalyst eddy flow activation recovering for being built in boiling bed hydrogenation reactor head
Device.
In the disclosure, the catalyst eddy flow activation recovering device by shell of column, the cone section being connect with shell of column, be placed in shell of column
Impeller guide ring, with cone section connect catalyst recurrent canal, connect with catalyst recurrent canal non-return guide cone, be placed in shell of column
Liquid phase overflow pipe that is interior and stretching out shell of column and the gas-liquid connecting with reactor head mix outlet pipe composition;Wherein, the liquid phase overflow
The upper surface of pipe is higher than the liquid level in the boiling bed hydrogenation reactor.
In the disclosure, it is living that 1 or more catalyst eddy flow in parallel is provided in the boiling bed hydrogenation reactor
Property restorer.
In the disclosure, the impeller guide ring is made of multiple swirl vanes, and the swirl vane is in the shell of column
Standoff height is the 5~20% of the height of the shell of column, and the tilt angle of the swirl vane relative level is 15~80 °,
There is fan-shaped overlapping region, and the central angle of the fan-shaped overlapping region is 1~10 ° between adjacent two pieces of swirl vanes.
In the disclosure, the impeller guide ring is made of one or more helical ducts.
In the disclosure, the upper end of the cone section connects the lower end of the shell of column, and the lower end for boring section connects the catalyst
The upper end of recurrent canal;Cone section is inverted conical, and axis is overlapped with the axis of the shell of column, the angle in bus same level face
It is 5~89 °.
In the disclosure, the boiling bed hydrogenation reactor shell is bored by coaxial lower part latus rectum section, middle part from bottom to top
Shape reducer and top expanding reach composition, the diameter of the top expanding reach are the 100~200% of lower part latus rectum section, and top is expanded
The height of big section is the 2~20% of lower part latus rectum section height;Middle part taper reducer is for connecting lower part latus rectum section and top
The inverted-cone shape of expanding reach, the angle in bus same level face are 30~60 °.
In the disclosure, the boiling bed hydrogenation reactor is used for containing aerobic, sulphur, nitrogen, chlorine and metal impurities atom
Hydrotreating, hydrofinishing and the hydrocracking process of macromolecule hydrocarbon, hydroconversion condition can be with are as follows: and operation temperature is 250~
500 DEG C, operating pressure is 5~30MPa, and reaction weight hourly space velocity is 0.2~4h-1, hydrogen to oil volume ratio is 200~3000.
Below referring to attached drawing.
Fig. 1 is that the boiling bed hydrogenation catalyst reactor eddy flow activity of a preferred embodiment according to the present invention is extensive
The structural schematic diagram of apparatus for coating.As shown in Figure 1, the boiling bed hydrogenation catalyst reactor eddy flow activity recovering device is main
It is made of boiling bed hydrogenation reactor shell 1 and the catalyst eddy flow activation recovering device 2 being built in shell 1;Other component is such as
Compared with boiling bed hydrogenation reactor it is the same, also have raw material oil-in 3, circulation oil-in 4, hydrogen inlet 5, gas-liquid distribution
The gentle liquid-phase product mixed export 7 of device 6;After entering boiling bed hydrogenation reactor after feedstock oil, recycle oil and hydrogen pressurization heating,
By gas-liquid distributor 6 it is uniformly distributed after form fluidized catalyst bed A, wherein there are bubbles;Even fluidizing catalyst granules
Form gas-liquid-solid three-phase mixture with liquid phase in reactor, gas phase, the three-phase mixture in boiling bed hydrogenation reactor always
Gas-liquid-solid three-phase admixture is kept, catalyst granules is in mixed and disorderly unordered motion state;The three-phase mixture arrives at boiling
After the liquid level B location of bed hydroprocessing reactor head, under the effect of gravity, gas phase deviates from three-phase mixture, anti-in boiling bed hydrogenation
The liquid level position top at the top of device is answered to form gas-phase space C.
Fig. 2 is that the boiling bed hydrogenation catalyst reactor eddy flow activity of a preferred embodiment according to the present invention is extensive
The structural schematic diagram of catalyst eddy flow activation recovering device in apparatus for coating.As shown in Fig. 2, the catalyst rotation being built in shell 1
Activation recovering device 2 is flowed by shell of column 8, cone section 9, impeller guide ring 10, catalyst recurrent canal 11, non-return guide cone 12, liquid phase overflow
Pipe 13 and gas-liquid are mixed outlet pipe 14 and are formed;The upper surface of the liquid phase overflow pipe 13 is higher than the liquid in the boiling bed hydrogenation reactor
Face height;The remaining liquid-solid two-phase mixture containing catalyst granules is opened by 8 upper end of shell of column of catalyst eddy flow activation recovering device 2
Mouth enters, and the rotational flow of the solid the two mixture of liquid is formed by 10 water conservancy diversion of impeller guide ring;Eddy flow flowing is presented in typical
The aggregate motion of portion's forced vortex, external semi-free vortex;Wherein, DcIndicate the diameter of shell 1, DhoIndicate that liquid phase product mix goes out
The diameter of mouth, D1Indicate the diameter of liquid phase overflow pipe 13, D2Indicate the diameter of shell of column 8, D3Indicate the straight of catalyst recurrent canal 11
Diameter, D4Indicate that gas-liquid mixes the diameter of outlet pipe 14, H1Indicate 8 upper surface distance of shell of column, H2Indicate the height of liquid phase overflow pipe 13, H3
Indicate the height of shell of column 8, H4Indicate 13 upper surface distance of liquid phase overflow pipe, H5Indicate that gas-liquid mixes the height of outlet pipe 14, H6Expression is urged
The height of agent recurrent canal 11, α indicate that the angle of cone section 8, β indicate the blade tilt of impeller guide ring 10.
Fig. 3 is tangential in combined vortex in the catalyst eddy flow activation recovering device of a preferred embodiment according to the present invention
VELOCITY DISTRIBUTION and catalyst granules are from, revolution motion schematic diagram.As shown in figure 3, catalyst granules is extensive in catalyst eddy flow activity
In multiple device will do revolution motion around the central axis of eddy flow activation recovering device, at the same catalyst granules also by around catalyst granules from
Body central axis is done rotation movement;When catalyst granules is in forced vortex, the sense of rotation of catalyst granules is the same as the side of revolution
To identical;When in catalyst granules processing semi-free vortex, the sense of rotation of catalyst granules is contrary with revolving;Due to
The presence of catalyst revolution motion, catalyst granules will be had the centre of eddy flow activation recovering device to move to side wall by centrifugal force effect
It moves;If catalyst granules moves in semi-free vortex from forced vortex, the sense of rotation of catalyst will change;Due to
Spinning motion also occurs for catalyst granules, so that the carbon distribution presoma in catalyst surface and duct while revolution motion
The operating on centrifugal force being subject to initial carbon alternately changes;Carbon distribution presoma in final catalyst surface and duct and initial
Carbon, so that the active sites in catalyst surface and duct expose again, reaches since alternate oscillation action removes
The purpose that catalyst activity restores;During catalyst eddy flow activation recovering, catalyst granules is due to revolution, by liquid-solid two-phase
Directional migration in mixture, and be enriched in the side wall of catalyst eddy flow activation recovering device, eventually pass through the return of catalyst recurrent canal
In the conversion zone of boiling bed hydrogenation reactor;Meanwhile be stripped of catalyst granules clarification liquid phase and gas-phase space in gas phase
Outlet pipe is mixed by gas-liquid as product after mixing, discharge boiling bed hydrogenation reactor is exported by liquid phase product mix;Wherein,
O indicates coordinate origin, 1 indicates the serial number of spherical particles, and 2 indicate the serial number of spherical particles, UtIndicate tangential velocity, R1Expression is urged
The radius of agent eddy flow activation recovering device, r indicate radius of the particle in catalyst eddy flow activation recovering device, r1Indicate serial number
Radius in catalyst eddy flow activation recovering device locating for 1 particle, r2Indicate catalyst eddy flow activity locating for the particle of serial number 2
Radius in restorer, rmIndicate the radius in catalyst eddy flow activation recovering device locating for the particle of serial number m, τ1Indicate serial number
Hydrodynamic shear suffered by particle for 1, τ2Indicate hydrodynamic shear suffered by the particle of serial number 2, τ1+ δ τ indicates serial number 1
Particle suffered by hydrodynamic shear and the hydrodynamic shear on particle diameter direction increment sum, ω1Indicate serial number 1
The rotational velocity of particle, ω2Indicate the rotational velocity of the particle of serial number 2.
Fig. 4 is the boiling bed hydrogenation catalyst reactor eddy flow activity of another preferred embodiment according to the present invention
The structural schematic diagram of recovery device.As shown in figure 4, the boiling bed hydrogenation catalyst reactor eddy flow activity recovering device master
It to be made of boiling bed hydrogenation reactor shell 1 and the catalyst being built in shell 1 eddy flow activation recovering device 2;Other component
As existing boiling bed hydrogenation reactor, also there is raw material oil-in 3, circulation oil-in 4, hydrogen inlet 5, gas-liquid point
The gentle liquid-phase product mixed export 7 of cloth device 6;Wherein, as shown in line A-A section, using four cyclone parallel connections, that is, 4 are used
Catalyst eddy flow activation recovering device is arranged in parallel.
Fig. 5 is according to the embodiment of the present application 1 using boiling bed hydrogenation catalyst reactor eddy flow activity of the invention
The process flow diagram of recovery device.As shown in figure 5, tap water, from sink b, tap water (is higher than through circulating pump c pressurization
Reactor pressure) after, reactor is entered by the mixed phase entrance of the bottom of boiling bed hydrogenation reactor a;Air warp in atmosphere
It is stored in air accumulator e after crossing air compressor machine d pressurization, air is exported by air accumulator e by the mixed of the bottom of boiling bed hydrogenation reactor a
Phase entrance enters reactor;Catalyst particles under the momentum transmitting effect of originally water and air, in boiling bed hydrogenation reactor a
Grain reaches fluidized state;Three phase separator of the gas-liquid-solid three-phase mixture Jing Guo reactor head point in fluidized bed reactor
From the gas phase of acquisition is exported by gas-liquid mixed phase after mixing with the liquid phase of acquisition and leads to fluidized bed reactor liquid phase products export;
The liquid-phase reflux of boiling bed hydrogenation reactor discharge is into sink b, and gas phase emission is into atmosphere.
Fig. 6 is according to the embodiment of the present application 2 using boiling bed hydrogenation catalyst reactor eddy flow activity of the invention
The process flow diagram of recovery device.As shown in fig. 6, feedstock oil and hydrogen supply agent by boiling bed hydrogenation reactor a bottom into
Enter reactor;Recycle oil is mutually exported from the oil of cold high pressure separator g, and recycle oil is pressurized to through circulating pump c higher than reactor
After interior pressure, same to hydrogen (including the recycle hydrogen from circulating hydrogen compressor and the new hydrogen from device for producing hydrogen) mixing;Recycle oil
After the heated furnace b1 heating of mixture of hydrogen, reactor is entered by the mixed phase entrance of the bottom of boiling bed hydrogenation reactor a;
Under the momentum transmitting effect of recycle oil and hydrogen, the catalyst granules in boiling bed hydrogenation reactor a reaches fluidized state;It is former
Catalytic hydrodeoxygenation reaction occurs in boiling bed hydrogenation reactor for material oil, and the oxygen atom in feedstock oil is with water (H2) and dioxy O
Change carbon (CO2) form removing, it obtains using alkane, aromatic hydrocarbons as the oil product of main component;It is completed in fluidized bed reactor plus hydrogen is de-
Three phase separator separation of the gas-liquid-solid three-phase mixture Jing Guo reactor head after oxygen reaction, the gaseous products of acquisition include anti-
The components such as carbon dioxide, vapor, the lighter hydrocarbons for answering device remaining hydrogen, reaction to generate include dissolution hydrogen with the liquid-phase product obtained
Alkane and aromatic component together through gas-liquid mix outlet pipe by boiling bed hydrogenation reactor gas-liquid products export be discharged;Ebullated bed adds
The gas-liquid two-phase product of hydrogen reactor discharge passes through high pressure hot separator d1 flash liberation, and the hot high score gas of acquisition goes to high pressure sky
Cooler f;Hot high score gas carries out de- liquid after high-pressure air cooler f is cooling, into cold high pressure separator g, obtains without drop
Cold high score gas;Cold high score gas passes through the separating-purifying of membrane separator i, obtains the higher circulating hydrogen of hydrogen purity;Circulating hydrogen
It pressurizes by air compressor machine j, is mixed with new hydrogen;The bottom cold high pressure separator g separation acquisition oil phase and water phase, water phase discharger,
For a part of oily phase as recycle oil Returning reactor, another part of oily phase goes to cold low separator h;It is obtained from hot high score
Hot high score oil goes to thermal low-pressure separators e1;It is separated through thermal low-pressure separators e1, the hot low point of gas of acquisition goes to cold low separation
The heat low oil of device h, acquisition go to fractionating system;In cold low separator h, separate acquisition cold low point of gas go to torch or
It is then used as fuel gas, the cold low oil of acquisition goes to fractionating system.
Fig. 7 is according to the embodiment of the present application 3 using boiling bed hydrogenation catalyst reactor eddy flow activity of the invention
The process flow diagram of recovery device.As shown in fig. 7, feedstock oil and hydrogen supply agent by boiling bed hydrogenation reactor a bottom into
Enter reactor;Recycle oil is mutually exported from the oil of cold high pressure separator g, and recycle oil is pressurized to through circulating pump c higher than reactor
After interior pressure, same to hydrogen (including the recycle hydrogen from circulating hydrogen compressor and the new hydrogen from device for producing hydrogen) mixing;Recycle oil
After the heated furnace b1 heating of mixture of hydrogen, reactor is entered by the mixed phase entrance of the bottom of boiling bed hydrogenation reactor a;
Under the momentum transmitting effect of recycle oil and hydrogen, the catalyst granules in boiling bed hydrogenation reactor a reaches fluidized state;It is former
Catalytic hydrodeoxygenation reaction occurs in boiling bed hydrogenation reactor for material oil, and the oxygen atom in feedstock oil is with water (H2) and dioxy O
Change carbon (CO2) form removing, it obtains using alkane, aromatic hydrocarbons as the oil product of main component;It is completed in fluidized bed reactor plus hydrogen is de-
Three phase separator separation of the gas-liquid-solid three-phase mixture Jing Guo reactor head after oxygen reaction, the gaseous products of acquisition include anti-
The components such as carbon dioxide, vapor, the lighter hydrocarbons for answering device remaining hydrogen, reaction to generate include dissolution hydrogen with the liquid-phase product obtained
Alkane and aromatic component together through gas-liquid mix outlet pipe by boiling bed hydrogenation reactor gas-liquid products export be discharged.Ebullated bed adds
The gas-liquid two-phase product of hydrogen reactor discharge passes through high pressure hot separator d1 flash liberation, and the hot high score gas of acquisition goes to high pressure sky
Cooler f;Hot high score gas carries out de- liquid after high-pressure air cooler f is cooling, into cold high pressure separator g, obtains without drop
Cold high score gas;Cold high score gas passes through the separating-purifying of membrane separator i, obtains the higher circulating hydrogen of hydrogen purity;Circulating hydrogen
It pressurizes by air compressor machine j, is mixed with new hydrogen;The bottom cold high pressure separator g separation acquisition oil phase and water phase, water phase discharger,
For a part of oily phase as recycle oil Returning reactor, another part of oily phase goes to cold low separator h;It is obtained from hot high score
Hot high score oil goes to thermal low-pressure separators e1;It is separated through thermal low-pressure separators e1, the hot low point of gas of acquisition goes to cold low separation
The heat low oil of device h, acquisition go to fractionating system;In cold low separator h, separate acquisition cold low point of gas go to torch or
It is then used as fuel gas, the cold low oil of acquisition goes to fractionating system.
Embodiment
Below with reference to specific embodiment, the present invention is further explained.It should be appreciated, however, that these embodiments are only used for
It is bright the present invention and be not meant to limit the scope of the invention.The test method of actual conditions is not specified in the following example, usually
According to normal conditions, or according to the normal condition proposed by manufacturer.Unless otherwise indicated, all percentage and number be by weight
Meter.
Embodiment 1:
One, device name
5000L/h boiling bed hydrogenation reactor cold model unit.
Two, process flow
As shown in Figure 5.Tap water from sink b, tap water after circulating pump c is pressurized and (is higher than reactor pressure),
Reactor is entered by the mixed phase entrance of the bottom of boiling bed hydrogenation reactor a;Air in atmosphere stores up after air compressor machine d pressurization
There are in air accumulator e, air enters reactor by the mixed phase entrance of the bottom of boiling bed hydrogenation reactor a by the outlet air accumulator e.
Under the momentum transmitting effect of originally water and air, the catalyst granules in boiling bed hydrogenation reactor a reaches fluidized state.?
Three phase separator separation of the gas-liquid-solid three-phase mixture Jing Guo reactor head, the gas phase and acquisition of acquisition in fluidized bed reactor
Liquid phase mixing after by gas-liquid mixed phase outlet lead to fluidized bed reactor liquid phase products export.The discharge of boiling bed hydrogenation reactor
Liquid-phase reflux into sink b, gas phase emission is into atmosphere.
Three, fluidized bed reactor structure size
Boiling bed hydrogenation reactor cold model unit structure size is as shown in table 1 below:
Table 1:5000L/h boiling bed hydrogenation reactor cold model unit structure size
Four, implementation result
The test process of 5000L/h boiling bed hydrogenation cold model unit uses originally water and air and is tested, and tests
As a result as shown in table 2 below.In terms of test result, catalyst reaches even fluidizing, and continuous operation 20 hours are without failure,
0.5mm catalyst taking-out amount is controlled less than 2.5 μ g/g.
Table 2:5000L/h boiling bed hydrogenation cold model unit test result
Embodiment 2:
One, device name
200L/h sludge lysate hydrogenation deoxidation device.
Two, process flow
As shown in Figure 6.Feedstock oil and hydrogen supply agent enter reactor by the bottom of boiling bed hydrogenation reactor a.Feedstock oil and
The control range of the feeding temperature of hydrogen supply agent is room temperature~45 DEG C, the mass ratio of general control hydrogen supply agent and feedstock oil is 0.25~
2:1.The boiling bed hydrogenation deoxidation product that the hydrogen supply agent may come from feedstock oil passes through diesel oil or wax that fractionation obtains
The diesel oil or wax oil distillate of oil distillate oil or the high arene content outside device.Recycle oil is separated from cold anticyclone
The oil of device g mutually exports, and after circulating pump c is pressurized to 8~20MPa (be higher than reactor pressure), same to hydrogen (including comes recycle oil
The recycle hydrogen of self-loopa hydrogen compressor and new hydrogen from device for producing hydrogen) mixing;The heated furnace of the mixture of recycle oil and hydrogen
After b1 is heated to 200~450 DEG C, reactor is entered by the mixed phase entrance of the bottom of boiling bed hydrogenation reactor a.In recycle oil and
Under the momentum transmitting effect of hydrogen, the catalyst granules in boiling bed hydrogenation reactor a reaches fluidized state.Feedstock oil is boiling
Catalytic hydrodeoxygenation reaction occurs in bed hydroprocessing reactor, the oxygen atom in feedstock oil is with water (H2) and carbon dioxide (CO O2) shape
Formula removing, obtains using alkane, aromatic hydrocarbons as the oil product of main component.Gas after completing hydrogenation deoxidation reaction in fluidized bed reactor
Liquid consolidates three phase separator separation of the three-phase mixture Jing Guo reactor head, and the gaseous products of acquisition include reactor residual hydrogen
The components such as carbon dioxide, vapor, the lighter hydrocarbons that gas, reaction generate include the alkane and virtue for dissolving hydrogen with the liquid-phase product obtained
The hydrocarbon component is mixed outlet pipe through gas-liquid together and is discharged by the gas-liquid products export of boiling bed hydrogenation reactor.Boiling bed hydrogenation reactor row
Gas-liquid two-phase product out passes through high pressure hot separator d1 flash liberation, and the hot high score gas of acquisition goes to high-pressure air cooler f;It is hot high
Divide gas after high-pressure air cooler f is cooled to 40~50 DEG C, carries out de- liquid into cold high pressure separator g, obtain without drop
Cold high score gas;Cold high score gas passes through the separating-purifying of membrane separator i, obtains the higher circulating hydrogen of hydrogen purity;Circulating hydrogen
It pressurizes by air compressor machine j, is mixed with new hydrogen.The bottom cold high pressure separator g separation acquisition oil phase and water phase, water phase discharger,
For a part of oily phase as recycle oil Returning reactor, another part of oily phase goes to cold low separator h.It is obtained from hot high score
Hot high score oil goes to thermal low-pressure separators e1.It is separated through thermal low-pressure separators e1, the hot low point of gas of acquisition goes to cold low separation
The heat low oil of device h, acquisition go to fractionating system.In cold low separator h, separate acquisition cold low point of gas go to torch or
It is then used as fuel gas, the cold low oil of acquisition goes to fractionating system.
Three, fluidized bed reactor structure size
Sludge lysate hydrogenation deoxidation device fluidized bed reactor structure size is as shown in table 3 below
Table 3:200L/h sludge lysate hydrogenation deoxidation device fluidized bed reactor structure size
Four, implementation result
The test process of 200L/h sludge lysate hydrogenation deoxidation device uses sewage treatment plant excess sludge lysate
It is tested with refinery " three mud " two kinds of feedstock oils of lysate, test result is as shown in table 4 below.In terms of test result, catalysis
Agent reaches even fluidizing, does not occur within continuous operation 2000 hours reactor coking, and 0.5mm catalyst taking-out amount is controlled less than 2.5 μ
g/g。
Table 4:200L/h sludge lysate hydrogenation deoxidation device experiment result
Embodiment 3:
One, device name
100L/h sawdust lysate hydrogenation deoxidation device
Two, process flow
As shown in Figure 7.Feedstock oil and hydrogen supply agent enter reactor by the bottom of boiling bed hydrogenation reactor a.Feedstock oil and
The control range of the feeding temperature of hydrogen supply agent is room temperature~45 DEG C, the mass ratio of general control hydrogen supply agent and feedstock oil is 0.25~
2:1.The boiling bed hydrogenation deoxidation product that the hydrogen supply agent may come from feedstock oil passes through diesel oil or wax that fractionation obtains
The diesel oil or wax oil distillate of oil distillate oil or the high arene content outside device.Recycle oil is separated from cold anticyclone
The oil of device g mutually exports, and after circulating pump c is pressurized to 8~20MPa (be higher than reactor pressure), same to hydrogen (including comes recycle oil
The recycle hydrogen of self-loopa hydrogen compressor and new hydrogen from device for producing hydrogen) mixing;The heated furnace of the mixture of recycle oil and hydrogen
After b1 is heated to 200~450 DEG C, reactor is entered by the mixed phase entrance of the bottom of boiling bed hydrogenation reactor a.In recycle oil and
Under the momentum transmitting effect of hydrogen, the catalyst granules in boiling bed hydrogenation reactor a reaches fluidized state.Feedstock oil is boiling
Catalytic hydrodeoxygenation reaction occurs in bed hydroprocessing reactor, the oxygen atom in feedstock oil is with water (H2) and carbon dioxide (CO O2) shape
Formula removing, obtains using alkane, aromatic hydrocarbons as the oil product of main component.Gas after completing hydrogenation deoxidation reaction in fluidized bed reactor
Liquid consolidates three phase separator separation of the three-phase mixture Jing Guo reactor head, and the gaseous products of acquisition include reactor residual hydrogen
The components such as carbon dioxide, vapor, the lighter hydrocarbons that gas, reaction generate include the alkane and virtue for dissolving hydrogen with the liquid-phase product obtained
The hydrocarbon component is mixed outlet pipe through gas-liquid together and is discharged by the gas-liquid products export of boiling bed hydrogenation reactor.Boiling bed hydrogenation reactor row
Gas-liquid two-phase product out passes through high pressure hot separator d1 flash liberation, and the hot high score gas of acquisition goes to high-pressure air cooler f;It is hot high
Divide gas after high-pressure air cooler f is cooled to 40~50 DEG C, carries out de- liquid into cold high pressure separator g, obtain without drop
Cold high score gas;Cold high score gas passes through the separating-purifying of membrane separator i, obtains the higher circulating hydrogen of hydrogen purity;Circulating hydrogen
It pressurizes by air compressor machine j, is mixed with new hydrogen.The bottom cold high pressure separator g separation acquisition oil phase and water phase, water phase discharger,
For a part of oily phase as recycle oil Returning reactor, another part of oily phase goes to cold low separator h.It is obtained from hot high score
Hot high score oil goes to thermal low-pressure separators e1.It is separated through thermal low-pressure separators e1, the hot low point of gas of acquisition goes to cold low separation
The heat low oil of device h, acquisition go to fractionating system.In cold low separator h, separate acquisition cold low point of gas go to torch or
It is then used as fuel gas, the cold low oil of acquisition goes to fractionating system.
Three, fluidized bed reactor structure size
Sawdust lysate hydrogenation deoxidation device fluidized bed reactor structure size is as shown in table 5 below.
Table 5:100L/h sawdust lysate hydrogenation deoxidation device
Four, implementation result
The test process of 100L/h sawdust lysate hydrogenation deoxidation device uses sawdust lysate and is tested, and tests
As a result as shown in table 6 below.In terms of test result, catalyst reaches even fluidizing, does not occur reactor within continuous operation 2500 hours
Coking, 0.6mm catalyst taking-out amount are controlled less than 1.5 μ g/g.
Table 6:100L/h sawdust lysate hydrogenation deoxidation device experiment result
Above-mentioned listed embodiment is only presently preferred embodiments of the present invention, implementation model not for the purpose of limiting the invention
It encloses.Equivalence changes and modification made by the content of i.e. all claims according to the present invention, all should be technology model of the invention
Farmland.
All references mentioned in the present invention is incorporated herein by reference, independent just as each document
It is incorporated as with reference to such.In addition, it should also be understood that, after reading the above teachings of the present invention, those skilled in the art can
To make various changes or modifications to the present invention, such equivalent forms equally fall within model defined by the application the appended claims
It encloses.