US3067130A - Platforming process - Google Patents
Platforming process Download PDFInfo
- Publication number
- US3067130A US3067130A US27639A US2763960A US3067130A US 3067130 A US3067130 A US 3067130A US 27639 A US27639 A US 27639A US 2763960 A US2763960 A US 2763960A US 3067130 A US3067130 A US 3067130A
- Authority
- US
- United States
- Prior art keywords
- catalyst
- feed
- sulfur
- platforming
- per pound
- 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
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G35/00—Reforming naphtha
- C10G35/04—Catalytic reforming
Definitions
- Platforming is herein defined as a catalytic reforming process in which a hydrocarbon fraction containing naphthenes and paraffins and boiling in the gasoline boiling range is contacted in the vapor phase and in the presence of a substantial pressure of hydrogen with a catalyst containing platinum on a suitable support such as alumina under dehydrogenating conditions of temperature e.g., 800l000 F., whereby a product of improved octane number is obtained.
- the severity of the Platforming operation is primarily a function of the temperature, pressure, and space velocity. Generally in commercial practice the severity is controlled by the temperature as explained above. The pressure and space velocity normally are not altered over any appreciable range in a given Platforming plant.
- the reaction temperature must be increased 10 F. in order to maintain a constant quality of the product. If the maximum temperature increase in such a case is 100 F. (e.g., 850 to 950 F.) it is seen that the maximum catalyst life under these conditions is 10 barrels per pound of catalyst.
- the decline rate is not necessarily constant throughout a run but is generally approximately In commercial practice there are three types of Platforming operations herein designated as continuous, semiregenerative and regenerative. As Will be evident from the above, when mild conditions (i.e., low severity) are sufficient to obtain a product of satisfactory octane number the catalyst decline rate is very low and the process may be operated continuously for many months producing dfiblfid Patented Dec. 4, 1962 the maximum quantity of product. In this case when the catalyst is spent it is replaced by a charge of fresh catalyst or catalyst that has been reworked in a separate plant. The cost of the catalyst is of the order of $5.00 per pound.
- the process of the present invention relates to semiregenerative Platforming. It has no application in continuous or regenerative Platforming.
- FIGURE 1 of the drawing is a graph showing the temperature required to provide 100 Fl0 Platformate vs. the catalyst age under semi-regenerative conditions.
- FIGURE 2 is a graph showing the debutanized Platformate yield vs. catalyst age in the same semi-regenerative runs.
- FIGURE 3 is a graph showing the sulfur content of the catalyst after use with a sulfur-containing feed and during subsequent treatment of a desulfurized feed.
- feeds were heavy naphthas having the properties shown in table 1.
- Example 1 In this example the catalyst was not presulfided and the desulfurized feed was Platforms-d under the stated conditions. The temperature was increased with time as shown by curve 1 in FIGURE 1 to maintain the production of platformate having an F-l-O octane number of 100. The yield of debutanized reformate declined as shown by curve 1 in FIGURE 2.
- Example 2 In this example the catalyst was presulfided by treatment with H S for 2 hours at 900 F. Thiophene was added to the feed to give 100 p.p.m. sulfur during the entire run. The results are shown in curve 2 of FIG- URES 1 and 2.
- Example 3 In this example the catalyst was not presulfided but thiophene equivalent to 300 p.p.m. of sulfur was added to the feed. After processing 5.4 barrels of feed per pound of catalyst a desulfurized feed was substituted for 2 barrels per pound. The results are shown in curve 3 in FIGURES 1 and 2.
- the catalyst in all runs was regenerable at the end of the runs. However, it should be noted that the catalyst in Example 3 would not be regenerable if the run Were stopped at 5.4 barrels per pound. The reason for this will be apparent from FIGURE 3.
- the catalyst was used in the treatment of a feed containing 300 p.p.m. sulfur and then analyzed for sulfur. A desulfurized feed was then treated with the same catalyst and its sulfur content periodically determined. As shown by the curve in FIGURE 3 the sulfur content of the catalyst comes to a new low equilibrium value but it requires about 2 barrels of the desulfurized feed per pound of catalyst to achieve this end. If the catalyst contains more than a few hundredths of a percent of sulfur it cannot be regenerated because during the burning, oxides of sulfur are formed which permanently impair the activity of the catalyst and which are corrosive to the metal walls of the reactor and auxiliary equipment.
- the amount of sulfur in the feed to the Platforming reaction zone should be at least 200 p.p.m. and preferably 300 p.p.m. based on the feed. This includes any sulfur introduced with the recycled hydrogen. Higher concentration up to 400 p.p.m. or even 500 p.p.m. may be used but are generally not recommended because most plants are not constructed of alloys which are sufiiciently resistant to corrosion.
- the specified high sulfur concentration is maintained throughout the run except for the last approximately 2 barrels per pound of catalyst in which a desulfurized feed is substituted.
- the sulfur-containing feed is used for about 13 barrels, per pound and the desulfurized feed is used during the period from 13 to 15 barrels per pound.
- the feed used during the last 2 barrels per pound should be desulfurized to a sulfur level not exceeding about 25 p.p.m.
- the catalyst is flushed of hydrocarbons, regenerated by burning off the carbonaceous deposits, and reused in a new run.
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- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL264542D NL264542A (US08197722-20120612-C00042.png) | 1960-05-09 | ||
BE603543D BE603543A (US08197722-20120612-C00042.png) | 1960-05-09 | ||
US27639A US3067130A (en) | 1960-05-09 | 1960-05-09 | Platforming process |
DES73876A DE1181355B (de) | 1960-05-09 | 1961-05-08 | Verfahren zur halb-regenerierenden Plat-formierung von Kohlenwasserstoffgemischen |
FR861117A FR1297783A (fr) | 1960-05-09 | 1961-05-08 | Procédé de reformage catalytique au platine, avec semi-régénération, de mélanges d'hydrocarbures |
GB16721/61A GB910494A (en) | 1960-05-09 | 1961-05-08 | Catalytic reforming of hydrocarbon mixtures |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US27639A US3067130A (en) | 1960-05-09 | 1960-05-09 | Platforming process |
Publications (1)
Publication Number | Publication Date |
---|---|
US3067130A true US3067130A (en) | 1962-12-04 |
Family
ID=21838905
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US27639A Expired - Lifetime US3067130A (en) | 1960-05-09 | 1960-05-09 | Platforming process |
Country Status (5)
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3435090A (en) * | 1964-12-28 | 1969-03-25 | Monsanto Co | Calcination of platinum-alumina catalyst for alkane dehydrogenation |
US3439061A (en) * | 1966-10-10 | 1969-04-15 | Shell Oil Co | Catalytic dehydrogenation of paraffins |
US3448036A (en) * | 1968-07-26 | 1969-06-03 | Universal Oil Prod Co | Continuous,low pressure catalytic reforming process with sulfur and halogen inclusion and water exclusion |
US3481861A (en) * | 1968-01-16 | 1969-12-02 | Universal Oil Prod Co | Regeneration of coke-deactivated catalyst containing a platinum group component and a sulfur component |
US3502573A (en) * | 1969-06-16 | 1970-03-24 | Universal Oil Prod Co | Continuous,low pressure catalytic reforming process with sulfur inclusion,water exclusion,and low space velocity |
US3515665A (en) * | 1969-07-17 | 1970-06-02 | Universal Oil Prod Co | Continuous low pressure catalytic reforming process with water and ammonia exclusion and programmed sulfur addition |
US3669874A (en) * | 1970-10-19 | 1972-06-13 | Phillips Petroleum Co | Method of increasing catalyst activity in sour crude catalytic reformers |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2861944A (en) * | 1955-06-29 | 1958-11-25 | Standard Oil Co | Conversion of methylcyclopentane to benzene |
GB826909A (en) * | 1957-12-23 | 1960-01-27 | Universal Oil Prod Co | Process for reforming hydrocarbon fractions boiling in the gasoline range |
US3006841A (en) * | 1953-09-16 | 1961-10-31 | Universal Oil Prod Co | Hydrocarbon conversion process |
-
0
- BE BE603543D patent/BE603543A/xx unknown
- NL NL264542D patent/NL264542A/xx unknown
-
1960
- 1960-05-09 US US27639A patent/US3067130A/en not_active Expired - Lifetime
-
1961
- 1961-05-08 GB GB16721/61A patent/GB910494A/en not_active Expired
- 1961-05-08 DE DES73876A patent/DE1181355B/de active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3006841A (en) * | 1953-09-16 | 1961-10-31 | Universal Oil Prod Co | Hydrocarbon conversion process |
US2861944A (en) * | 1955-06-29 | 1958-11-25 | Standard Oil Co | Conversion of methylcyclopentane to benzene |
GB826909A (en) * | 1957-12-23 | 1960-01-27 | Universal Oil Prod Co | Process for reforming hydrocarbon fractions boiling in the gasoline range |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3435090A (en) * | 1964-12-28 | 1969-03-25 | Monsanto Co | Calcination of platinum-alumina catalyst for alkane dehydrogenation |
US3439061A (en) * | 1966-10-10 | 1969-04-15 | Shell Oil Co | Catalytic dehydrogenation of paraffins |
US3481861A (en) * | 1968-01-16 | 1969-12-02 | Universal Oil Prod Co | Regeneration of coke-deactivated catalyst containing a platinum group component and a sulfur component |
US3448036A (en) * | 1968-07-26 | 1969-06-03 | Universal Oil Prod Co | Continuous,low pressure catalytic reforming process with sulfur and halogen inclusion and water exclusion |
US3502573A (en) * | 1969-06-16 | 1970-03-24 | Universal Oil Prod Co | Continuous,low pressure catalytic reforming process with sulfur inclusion,water exclusion,and low space velocity |
US3515665A (en) * | 1969-07-17 | 1970-06-02 | Universal Oil Prod Co | Continuous low pressure catalytic reforming process with water and ammonia exclusion and programmed sulfur addition |
US3669874A (en) * | 1970-10-19 | 1972-06-13 | Phillips Petroleum Co | Method of increasing catalyst activity in sour crude catalytic reformers |
Also Published As
Publication number | Publication date |
---|---|
BE603543A (US08197722-20120612-C00042.png) | |
GB910494A (en) | 1962-11-14 |
DE1181355B (de) | 1964-11-12 |
NL264542A (US08197722-20120612-C00042.png) |
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