US2482140A - Method for hydrocarbon conversion - Google Patents
Method for hydrocarbon conversion Download PDFInfo
- Publication number
- US2482140A US2482140A US100417A US10041749A US2482140A US 2482140 A US2482140 A US 2482140A US 100417 A US100417 A US 100417A US 10041749 A US10041749 A US 10041749A US 2482140 A US2482140 A US 2482140A
- Authority
- US
- United States
- Prior art keywords
- particles
- bed
- hydrocarbon
- contact material
- coke
- 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.)
- Expired - Lifetime
Links
- 229930195733 hydrocarbon Natural products 0.000 title description 19
- 150000002430 hydrocarbons Chemical class 0.000 title description 19
- 239000004215 Carbon black (E152) Substances 0.000 title description 16
- 238000006243 chemical reaction Methods 0.000 title description 16
- 238000000034 method Methods 0.000 title description 6
- 239000000463 material Substances 0.000 description 20
- 239000002245 particle Substances 0.000 description 18
- 239000007788 liquid Substances 0.000 description 10
- 239000000571 coke Substances 0.000 description 8
- 230000005484 gravity Effects 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000005336 cracking Methods 0.000 description 4
- 238000005054 agglomeration Methods 0.000 description 3
- 230000002776 aggregation Effects 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 238000009827 uniform distribution Methods 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000009834 vaporization Methods 0.000 description 2
- 230000008016 vaporization Effects 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000004523 catalytic cracking Methods 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000004939 coking Methods 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000012084 conversion product Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000002006 petroleum coke Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 239000011269 tar Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
- B01J8/08—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with moving particles
- B01J8/12—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with moving particles moved by gravity in a downward flow
Definitions
- This invention relates to hydrocarbon conver-- sion and in particular to the formation of coke concurrently with the vaporization and cracking of heavy hydrocarbons such as bottoms and by drocarbcn residuals wherein the coke formed in the aforesaid reaction is deposited on discrete particles of a free-flowing non-agglomerating bed moving continuously by gravity alone.
- It is a continuation-impart or" my ccpending application Serial No. 537,767, filed February 13, 1945, and entitled. Improvements in converting hydro carbons, and a division of my copending application Serial No. 29,751, filed May 28, ill-l8, and entitled Hydrocarbon conversion.
- Fig. l is a schematic vertical section of a part of a reaction unit showing one form of liquid distributing means
- Fig. 2 is a vertical cross section on the line 2-2 of Figure l on an enlarged scale.
- Figure i. represents a pilot plant size unit the main body ill of which consists of a tube of nominal diameter surmounted by a hopper top generally indicated at it through which projects the contact material inlet pipe i i.
- the contact material in turn is contained in a hopper i6 and the contact material in passing through the inlet pipe ll into the large chamber ill will form a flowing pile of material the outline of which is shown at it.
- the angle of this pile or mass is a function of the angle of repose of the material.
- a vapor releasing space generally indicated at it from which the vapors may be removed through the line 22.
- control valve 23 is provided in the outlet pipe.
- the feed spreader or distributor in the present tube ll As shown in large cross section in Figure 2, the openings are on an angle so that the contact material which passes down through the conduit I4 and as it flows into the piles l8, will be completely coated with the charge.
- the hydrocarbon inlet is indicated at 28.
- the discrete particles of contact material may be either inert porous contact material such as Koppers coke, petroleum coke, Alundum, Carborundum, or other materials or, alternatively, it maybe of a catalytic type such as silica gel or other known catalyst depending upon the reaction desired.
- the bed particles are maintained in a range offrom 1 in, to /4 in. major dimension and they may be in lump, pellet or extruded form;
- it is suflicient if they are introduced in the inlet is at a temperature at from 800 F. to 1300 F.
- the hydrocarbons will, of course, be introduced at a suitable temperature in the usual range of 700 F. to 900 F.
- the vapors under such conditions will be of prime value for further cracking, usually having a gas oil composition with low carbon content so that they may be directly introduced into a conventional catalytic cracking unit for the production of high grade gasoline. If a cracking reaction is desired, the contact material being catalytic, and the temperatures and charge being adjusted accordingly, the, vapors will of course be of high quality gasoline type.
- the reaction is carried out at relatively low pressures which may range between 2 pounds p. s. i. g. and 60 pounds p. s. i. g.largely depending upon the pressure required to convey the nroduct vapors to subsequent process equipmen I
- a part thereof is flashed off" or evaporated upon contact with the hot bed particles and withdrawn as useful vapors which may be taken 01?, for further processing, to any suitable station.
- the remainder of the feed which does not flash oil or evaporate is taken up or received by particles substantially entirely whereby formation of sticky films between the discrete bed particles suflicient in depth or thickness to destroy the free flowing properties of the bed is totally obviated.
- An entirely impervious material such as beach gravel will ordinarily receive about 10% by weight of hydrocarbon under, my operating conditions.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
Sept. 20, 1949.
A. H. SCHUTTE METHOD FOR HYDROCARBON CONVERSION Original Filed May 28, .1948
INVENTOR. Mmskmyfifialle BY 3! E a z ATTORNEY Patented Sept. 20, 1949 M'EHQED FfiR HYDRGCARBON CONVEREEGN August Henry Schutte, Hastings on Hudson, N. if asslgnor to The hummus Company, New York, N. Y., a corporation of Delaware ()rlginal application May 28, 1948, i'slcriall No. 29,751. Divided and this application dune 21. 1949, erial No. Nib-ill? WE. 198 b?) it @llaims.
This invention relates to hydrocarbon conver-- sion and in particular to the formation of coke concurrently with the vaporization and cracking of heavy hydrocarbons such as bottoms and by drocarbcn residuals wherein the coke formed in the aforesaid reaction is deposited on discrete particles of a free-flowing non-agglomerating bed moving continuously by gravity alone. It is a continuation-impart or" my ccpending application Serial No. 537,767, filed February 13, 1945, and entitled. Improvements in converting hydro= carbons, and a division of my copending application Serial No. 29,751, filed May 28, ill-l8, and entitled Hydrocarbon conversion.
It is an object of this invention to make novel provision for the uniform distribution or liquids on the particles of the continuously moving gravity packed bed of contact material which moves downward through a sealed reaction chamber solely by gravity.
It is a further object of this invention to provide a new and improved method for securing the conversion of a hydrocarbon liquid in the presence of a continuously moving bed of contact material wherein the particles are uniformly coated with the non-vaporlzable portion of the hydrocarbon.
Further objects and advantages of my invention will appear from the following description of preferred forms of embodiment thereof taken in connection with the attached drawings in which:
Fig. l is a schematic vertical section of a part of a reaction unit showing one form of liquid distributing means; and
Fig. 2 is a vertical cross section on the line 2-2 of Figure l on an enlarged scale.
in accordance with my above mentioned appli cation and as pointed out in a copending application Serial No. 3,747, filed January 22, 1948, such application being a continuation-in-part of an earlier application Serial No. 510,119, filed November 13, 1943, and now abandoned, of which I am a coinventor, the disposition of heavy hydrocarbon by-products of cracking, distillation and like operations, comprising bottoms, tars and the like has represented a major operating problem in the petroleum industry. While it has been recognized that the conversion of a part of these by-products to coke along with the formation of useful and valuable conversion products would solve this problem, at least to a large degree, all former attempts have resulted in the use of expensive, complicated and cumbersome mechanlsms dificult to service and of relatively low emciency.
The present invention is particularly adapted to the uniform distribution of these heavy hydrocarbon feeds in liquid or substantially liquid form into a compact, iree==fiowlng gravity packed bed made up of discrete porous solid particles which move downward solely by gravity and in which the control of temperature and rate of feed of the charge and temperature and rate of feed of the bed, as well as the provision of a predetermined length of travel for bed particles, is so arranged as to avoid agglomeration. It has thus been found possible to obtain the continuous desired vaporization of the lighter portions of the charge and to form a coke coating on the discrete particles.
It is to be noted, however, that the uniform distribution of the charge is of substantial importance for if agglomeration occurs the bed stops moving and local low temperatures develop and the entire mass may tend to stop flowing.
I have found that it is desirable to avoid the introduction of any air or oxygen containing gas into the reaction chamber to prevent the forma tlon of combustion products which would tend to dilute the vapors resulting from the hydro carbon conversion. It is also not only unnecessary but undesirable to increase the temperature of the bed as it flows downward by gravity and preferably the hotter portion should be established at the top so that there is no tendency of the rising vapors to condense and coke on the surface of the reactor.
More particularly, referring to the drawings, Figure i. represents a pilot plant size unit the main body ill of which consists of a tube of nominal diameter surmounted by a hopper top generally indicated at it through which proiects the contact material inlet pipe i i. The contact material in turn is contained in a hopper i6 and the contact material in passing through the inlet pipe ll into the large chamber ill will form a flowing pile of material the outline of which is shown at it. The angle of this pile or mass is a function of the angle of repose of the material.
Between the top of the pile l8 and the dome of the hopper i2 is a vapor releasing space generally indicated at it from which the vapors may be removed through the line 22. It will, of course,
.be understood that the contact material moves downward by gravity out the bottom of the tube ill. Usually a control valve 23 is provided in the outlet pipe.
The feed spreader or distributor in the present tube ll. As shown in large cross section in Figure 2, the openings are on an angle so that the contact material which passes down through the conduit I4 and as it flows into the piles l8, will be completely coated with the charge. The hydrocarbon inlet is indicated at 28.
It will thus appear that the feed is applied to opposite sides of the stream of the discrete bed particles while said particles are confined in the inlet pipe I and when they are undergoing movement in the flowing piles from the material inlet to the reactor chamber i0. Uniformity of feed is assured; no liquid will be thrown against the construction is simple and effective and the feed openings are continuously kept clean by the movement of the particles across their surface.
The discrete particles of contact material may be either inert porous contact material such as Koppers coke, petroleum coke, Alundum, Carborundum, or other materials or, alternatively, it maybe of a catalytic type such as silica gel or other known catalyst depending upon the reaction desired. Preferably, the bed particles are maintained in a range offrom 1 in, to /4 in. major dimension and they may be in lump, pellet or extruded form; For the conversion of heavy hydrocarbons, it is suflicient if they are introduced in the inlet is at a temperature at from 800 F. to 1300 F. The hydrocarbons will, of course, be introduced at a suitable temperature in the usual range of 700 F. to 900 F. The vapors under such conditions will be of prime value for further cracking, usually having a gas oil composition with low carbon content so that they may be directly introduced into a conventional catalytic cracking unit for the production of high grade gasoline. If a cracking reaction is desired, the contact material being catalytic, and the temperatures and charge being adjusted accordingly, the, vapors will of course be of high quality gasoline type.
Ordinarily the reaction is carried out at relatively low pressures which may range between 2 pounds p. s. i. g. and 60 pounds p. s. i. g.largely depending upon the pressure required to convey the nroduct vapors to subsequent process equipmen I Upon spreading the feed upon the bed particles a part thereof is flashed off" or evaporated upon contact with the hot bed particles and withdrawn as useful vapors which may be taken 01?, for further processing, to any suitable station. The remainder of the feed which does not flash oil or evaporate is taken up or received by particles substantially entirely whereby formation of sticky films between the discrete bed particles suflicient in depth or thickness to destroy the free flowing properties of the bed is totally obviated. As much as of oil by weight to contact material may be applied without causing agglomeration depending upon the nature of the contact material. An entirely impervious material such as beach gravel will ordinarily receive about 10% by weight of hydrocarbon under, my operating conditions.
As these loaded bed particles pass downwardly by gravity as a column of greater horizontal cross sectional area than the streams through the body of the reactor i0, sufficient residence time is provided for the coking reaction to proceed to completion or, in other words, for the liquid hydrocarbon load on the particles to be thermally converted or cracked into lighter hydrocarbon vapors which pass up through the bed to the vapor outlet 22, leaving a residue of dry coke deposit. The particles in this condition pass out of the reactor through the outlet 23. This residence time at the normal operating temperatures may range from 10 to 30 minutes. In such case a depth of bed below the feed point must be provided which-is greater than the free flowing depth of the charge which at the temperatures under consideration has a viscosity of about one tenth that of water. A minimum depth of five feet and a preferred depth of thirty to fifty feet is the range for most effective dry coke formation.
While I have shown and described a preferred form of embodiment of my invention, 1' am aware that modifications may be made thereto and I therefore desire a broad interpretation of my invention within the scope and spirit of the description hereinv and of the claims appended hereinticle form solid contact mass material moving jecting a stream of high boiling liquid hydrocarbon charge into said stream near the lower end thereof.
2. The process as defined in claim 1 in which a plurality of streams of high boiling liquid hydrocarbon charge are injected into said stream of contact material at peripherally spaced points near the lower end thereof.
3. The process as'defined in claim 1 in which a plurality of streams of high boiling liquid hydrocarbon charge are injected into opposite sides of said stream of contact material at points above the loweren'd thereof.
AUGUST HENRY SCHU'I'I'E.
No references cited.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US100417A US2482140A (en) | 1948-05-28 | 1949-06-21 | Method for hydrocarbon conversion |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US29751A US2482139A (en) | 1948-05-28 | 1948-05-28 | Hydrocarbon conversion |
| US100417A US2482140A (en) | 1948-05-28 | 1949-06-21 | Method for hydrocarbon conversion |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2482140A true US2482140A (en) | 1949-09-20 |
Family
ID=26705302
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US100417A Expired - Lifetime US2482140A (en) | 1948-05-28 | 1949-06-21 | Method for hydrocarbon conversion |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2482140A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2701788A (en) * | 1951-03-10 | 1955-02-08 | Lummus Co | Coking of hydrocarbons |
| US2800432A (en) * | 1951-02-14 | 1957-07-23 | Houdry Process Corp | Contacting liquid hydrocarbons in a moving bed hydrocarbon conversion system |
| US2923677A (en) * | 1958-09-18 | 1960-02-02 | Socony Mobil Oil Co Inc | Method and apparatus for the supply of hydrocarbon charge to conversion reactors |
| US11207651B2 (en) | 2019-06-24 | 2021-12-28 | Exxonmobil Research And Engineering Company | Moving bed reactor for processing three phase flows |
| US11213796B2 (en) * | 2019-06-24 | 2022-01-04 | Exxonmobil Research And Engineering Company | Feed distribution apparatus for moving bed reactor |
| US11383202B2 (en) | 2019-06-24 | 2022-07-12 | ExxonMobil Technology and Engineering Company | Distillate production from oxygenates in moving bed reactors |
-
1949
- 1949-06-21 US US100417A patent/US2482140A/en not_active Expired - Lifetime
Non-Patent Citations (1)
| Title |
|---|
| None * |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2800432A (en) * | 1951-02-14 | 1957-07-23 | Houdry Process Corp | Contacting liquid hydrocarbons in a moving bed hydrocarbon conversion system |
| US2701788A (en) * | 1951-03-10 | 1955-02-08 | Lummus Co | Coking of hydrocarbons |
| US2923677A (en) * | 1958-09-18 | 1960-02-02 | Socony Mobil Oil Co Inc | Method and apparatus for the supply of hydrocarbon charge to conversion reactors |
| US11207651B2 (en) | 2019-06-24 | 2021-12-28 | Exxonmobil Research And Engineering Company | Moving bed reactor for processing three phase flows |
| US11213796B2 (en) * | 2019-06-24 | 2022-01-04 | Exxonmobil Research And Engineering Company | Feed distribution apparatus for moving bed reactor |
| US11383202B2 (en) | 2019-06-24 | 2022-07-12 | ExxonMobil Technology and Engineering Company | Distillate production from oxygenates in moving bed reactors |
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