WO1996009891A1 - A method for the demercaptanization of petroleum distillates - Google Patents
A method for the demercaptanization of petroleum distillates Download PDFInfo
- Publication number
- WO1996009891A1 WO1996009891A1 PCT/US1995/012339 US9512339W WO9609891A1 WO 1996009891 A1 WO1996009891 A1 WO 1996009891A1 US 9512339 W US9512339 W US 9512339W WO 9609891 A1 WO9609891 A1 WO 9609891A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- copper
- mass
- iron
- catalyst
- water
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- 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
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
-
- 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
- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
- B01J21/18—Carbon
-
- 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
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/50—Catalysts, in general, characterised by their form or physical properties characterised by their shape or configuration
- B01J35/58—Fabrics or filaments
-
- 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
- C10G27/00—Refining of hydrocarbon oils in the absence of hydrogen, by oxidation
- C10G27/04—Refining of hydrocarbon oils in the absence of hydrogen, by oxidation with oxygen or compounds generating oxygen
-
- 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
- C10G27/00—Refining of hydrocarbon oils in the absence of hydrogen, by oxidation
- C10G27/04—Refining of hydrocarbon oils in the absence of hydrogen, by oxidation with oxygen or compounds generating oxygen
- C10G27/10—Refining of hydrocarbon oils in the absence of hydrogen, by oxidation with oxygen or compounds generating oxygen in the presence of metal-containing organic complexes, e.g. chelates, or cationic ion-exchange resins
Definitions
- the invention relates to the field of the removal of mercaptan sulfur from petroleum distillates by means of oxidation, and may be used in the oil refining industry for the demercaptanization of gasoline, kerosene, and diesel fractions.
- the method which most closely resembles the method described herein is the method for the demercaptanization of high-boiling-point petroleum distillates by means of mercaptan oxidation using the oxygen of the air, in the presence of a 5% to 20% solution containing an alkali and a heterogeneous phthalocyanine catalyst, comprising cobalt phthalocyanine in an amount ranging from 0.005 to 0.9 mass %, deposited on a carbonaceous fibrous material in the form of a carbonaceous or graphite fiber.
- the objective of the present invention consists in achieving an increase in the degree of demercaptanization of petroleum distillates, an increase in the stability of the catalytic activity of the catalyst, and the elimination of the necessity of using significant quantities of the base.
- a method for the demercaptanization of mercaptan- containing petroleum distillates by means of the oxidation of said mercaptans with the oxygen of the air in the presence of a heterogeneous catalyst comprising contacting said mercaptans with oxygen in the presence of a catalyst comprising a water-soluble salt of copper, iron, nickel, or cobalt, in an amount ranging from about 0.01 to about 10.0 mass %, which is deposited onto a fibrous carbonaceous material, said material containing oxides of metals of variable valence; said method being carried out at a temperature falling within the range of about 80° to about 200 ⁇ C.
- a catalyst comprising a fibrous carbonaceous material containing oxides of metals of variable valence, and having deposited on said material, in an amount from about 0.01 to about 10.0 mass %, a water-soluble salt of copper, iron, nickel or cobalt.
- the stated objective is achieved by providing a method for the demercaptanization of petroleum distillates by means of the oxidation of mercaptans using the oxygen of the air, in the presence of a heterogeneous catalyst.
- a water-soluble salt of copper, iron, nickel, or cobalt may be used, in an amount ranging from 0.01 to 10.0 mass %, deposited on a fibrous carbon material in the form of a fabric-type material, felt, or rope, containing oxides of metals of variable valence, the process being carried out at a temperature ranging from about 80° to about 220°C.
- a carbonaceous fibrous material is used, containing oxides of calcium, magnesium, copper, manganese, iron, zinc and aluminum, in quantities which provide sufficient basicity for the oxidation of the mercaptans to occur. Typically, this amount will be up to about 0.03 mass %.
- the distinguishing features of the proposed method consist in the use of a heterogeneous catalyst, containing from about 0.01 to about 10.0 mass % of a water-soluble salt of copper, iron, nickel, or cobalt, on a material which consists of carbonaceous fibers; the use of a carbonaceous fibrous material in the form of a woven fabric (cloth) , felt, or rope (twisted strand) , containing the oxides of the above mentioned metals of variable valence in an amount of up to about 0.03 mass %; and the performance of the process at a temperature ranging from about 80° to about 220°C.
- water-soluble salts of copper, iron, nickel, and cobalt include, but are not limited to, salts of inorganic acids such as the sulfates, chlorides and nitroxides (nitrates) of these metals.
- Phenylates i.e., Ph-O-Me-O-Ph where Me is the metal and Ph is phenyl
- copper sulfate, copper chloride, copper phenylate, iron sulfate, nickel nitroxide and cobalt nitroxide are useful in the practice of this invention, with copper phenylate being particularly preferred because it does not carry over into the demercaptanized product.
- the proposed content of the water-soluble salt of Cu, Fe, Ni, or Co on the carbonaceous fibrous material in an amount ranging from 0.01 to 10.0 mass % is both necessary and sufficient, since with a content of the water-soluble salt of copper, iron, nickel, or cobalt which is less than 0.01 mass %, the required degree of mercaptan oxidation is not achieved.
- the higher limit for the content of a water-soluble salt of copper, iron, nickel, or cobalt (10.0 mass %) is determined by the adsorptive properties of the carbonaceous fibrous material with respect to the water-soluble salt of copper, iron, nickel, or cobalt.
- Typical oxides of metals of variable valence which are useful in this invention include, but are not limited to, oxides of calcium, magnesium, iron, manganese, copper, zinc and aluminum. Generally, these oxides are considered to but water-insoluble or only slightly soluble in water.
- Carbonaceous fibrous materials in the form of a woven fabric, felt, or rope (twisted strand) , containing the oxides of metals of variable valence in an amount of up to about 0.03 mass % are industrially produced by a process involving the soaking of the material in solutions of salts of the aforesaid metals, with their subsequent thermal treatment.
- the preparation of the proposed catalyst is carried out in accordance with the known method of soaking a carbonaceous fibrous material containing oxides of calcium, magnesium, copper, manganese, iron, zinc, and aluminum in aqueous solutions of the salts of copper, iron, nickel, or cobalt, at the required concentration, with subsequent drying.
- the proposed method has found approbation under laboratory conditions in examples involving the demercaptanization of a model mixture of dodecylmercaptan in dodecane, a gasoline fraction (boiling-off range 60° to 180°C) , a kerosene fraction 120° to 240°C) , and a diesel fraction (180° to 350°C) .
- a heterogeneous catalyst containing 10 mass % copper sulfate on a carbonaceous fabric which further contains oxides of calcium, magnesium, copper, manganese, iron, zinc, and aluminum in a quantity of 0.03 mass % are loaded into a batch reactor.
- the copper sulfate is deposited onto the carbonaceous fabric by the method of soaking to saturation using an aqueous solution.
- 35 ml of a model solution of n-dodecylmercaptan in dodecane are loaded into the reactor.
- the reactor constitutes a cylindrical vessel made of glass, having a capacity of 100 ml, heated from the outside by a metallic spiral. Air is supplied to the reactor from the bottom; this air is evenly distributed within the reactor space due to the Schott filter which has been installed in the lower part of the reactor.
- the oxidation of the mercaptans is carried out with the oxygen of the air, at a temperature of 100°C and atmospheric pressure, with air being supplied at a rate of 0.5 1/min. The time of oxidation is 4 minutes.
- the mercaptan sulfur content in the starting and refined raw material is determined by method of potentiometric titration.
- the demercaptanization of a model mixture of dodecylmercaptan in dodecane is carried out by a method similar to the one described for Example 1.
- the composition of the catalyst and the results of the experiment are given in Table 1.
- Example 2 Under the same conditions as those described in Example 1, in the presence of a heterogeneous catalyst which contained l mass % copper sulfate on a carbonaceous fabric containing 0.03 mass % of the oxides of metals indicated in Example 1, at a temperature of 220°C, over a period of 5 minutes, the demercaptanization of a diesel fraction having a mercaptan sulfur content equal to 0.02 mass % is carried out. Analysis of the de ercaptanized diesel fraction showed the residual content of mercaptan sulfur to be 0.0005 mass %. At the same time, the degree of oxidation of mercaptans in the diesel fraction constitutes 97.5%.
- Example 2 Under the same conditions as those described in Example 1, in the presence of a known heterogeneous catalyst which contains 0.5 mass % of cobalt disulophthalocyanine on a carbonaceous fabric (without oxides of metals) and a 20% alkali solution, at a temperature of 220°C, over a period of 5 minutes, the demercaptanization of a diesel fraction with a mercaptan sulfur content equal to 0.02 mass % is carried out. Analysis of the demercaptanized diesel fraction showed the residual content of mercaptan sulfur to be 0.0075 mass %. At the same time, the degree of oxidation of mercaptans in the diesel fraction constitutes 62.5%.
- the demercaptanization of a gasoline fraction having a mercaptan sulfur content of 0.077 mass % is carried out.
- Analysis of the demercaptanized fraction indicated the residual content of mercaptan sulfur to be 0.0001 mass %.
- the degree of oxidation of the mercaptans in the gasoline fraction constitutes 99.87%.
- Example 2 Under the same conditions as those described in Example 1, in the presence of a known heterogeneous catalyst which contains 0.5 mass % of cobalt disulophthalocyanine on a carbonaceous fabric (without oxides of metals) and a 20% alkali solution, at a temperature of 80°C, over a period of time lasting 3 minutes, the demercaptanization of a gasoline fraction with a mercaptan sulfur content of 0.077 mass % is carried out.
- a known heterogeneous catalyst which contains 0.5 mass % of cobalt disulophthalocyanine on a carbonaceous fabric (without oxides of metals) and a 20% alkali solution, at a temperature of 80°C, over a period of time lasting 3 minutes.
- the degree of mercaptan oxidation in the gasoline fraction constitutes 63.6%.
- the following example illustrates the preservation of high catalytic activity after prolonged use of the catalyst.
- a kerosene fraction 120 + 240 originating from the petroleum refinery of Ryazan, having a content of mercaptan sulfur of 0.0082% mass %, is subjected to demercaptanization over a period of 10 minutes.
- the purified kerosene is drained off, and a fresh portion of kerosene is poured into the reactor and subjected to oxidation. The process is repeated for several tens of cycles.
- the demercaptanization of a kerosene fraction is carried out in the presence of a known catalyst. The results of the experiment are given in Table 2.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Materials Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Catalysts (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Working-Up Tar And Pitch (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Claims
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| MX9702145A MX9702145A (en) | 1994-09-27 | 1995-09-26 | A method for the demercaptanization of petroleum distillates. |
| EP95934553A EP0783369A4 (en) | 1994-09-27 | 1995-09-26 | A method for the demercaptanization of petroleum distillates |
| AU36861/95A AU3686195A (en) | 1994-09-27 | 1995-09-26 | A method for the demercaptanization of petroleum distillates |
| NO971379A NO971379D0 (en) | 1994-09-27 | 1997-03-24 | Process for Demercaptanization of Petroleum Distillates |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/313,635 US5741415A (en) | 1994-09-27 | 1994-09-27 | Method for the demercaptanization of petroleum distillates |
| US08/313,635 | 1994-09-27 | ||
| RU940392/38 | 1994-10-18 | ||
| RU94039238A RU2076892C1 (en) | 1994-10-18 | 1994-10-18 | Method of demercaptanization of oil distillates |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO1996009891A1 true WO1996009891A1 (en) | 1996-04-04 |
Family
ID=26653803
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US1995/012339 Ceased WO1996009891A1 (en) | 1994-09-27 | 1995-09-26 | A method for the demercaptanization of petroleum distillates |
Country Status (7)
| Country | Link |
|---|---|
| EP (1) | EP0783369A4 (en) |
| CN (1) | CN1071136C (en) |
| AU (1) | AU3686195A (en) |
| CA (1) | CA2199373A1 (en) |
| MX (1) | MX9702145A (en) |
| NO (1) | NO971379D0 (en) |
| WO (1) | WO1996009891A1 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005116169A1 (en) * | 2004-05-31 | 2005-12-08 | Agency For Science, Technology And Research | Novel process for removing sulfur from fuels |
| US8016999B2 (en) | 2004-05-31 | 2011-09-13 | Agency For Science, Technology And Research | Process for removing sulfur from fuels |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1067709C (en) * | 1998-10-23 | 2001-06-27 | 中国石化广州石油化工总厂 | Process of demercaptaning for gasoline by catalyst cracking |
| KR100779124B1 (en) * | 2003-09-16 | 2007-11-28 | 쇼와 덴코 가부시키가이샤 | Composite of vapor grown carbon fiber and inorganic fine particle and use thereof |
| CN1320958C (en) * | 2005-05-30 | 2007-06-13 | 北京三聚环保新材料有限公司 | Double-effect catalyst and its production process |
| US9068128B2 (en) * | 2011-10-18 | 2015-06-30 | Baker Hughes Incorporated | Method for reducing hydrogen sulfide evolution from asphalt and heavy fuel oils |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3029201A (en) * | 1959-12-28 | 1962-04-10 | Universal Oil Prod Co | Water treatment |
| US4028269A (en) * | 1975-08-21 | 1977-06-07 | Uop Inc. | Process for the preparation of a solid bed catalyst system |
| US4364843A (en) * | 1979-11-28 | 1982-12-21 | Uop Inc. | Catalytic composite, method of manufacture, and process for use |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4672047A (en) * | 1984-03-08 | 1987-06-09 | Travis Chandler | Mercaptan oxidation catalyst |
| FR2601263B1 (en) * | 1986-07-11 | 1988-11-25 | Total France | NEW CATALYTIC COMPOSITE PRODUCT FOR THE OXIDATION OF MERCAPTANS AND ITS USE FOR THE SOFTENING OF OIL CUTTINGS. |
| JPS63283750A (en) * | 1987-05-14 | 1988-11-21 | Asahi Chem Ind Co Ltd | Catalyst using carbon fiber as carrier |
| JPH05184940A (en) * | 1992-01-14 | 1993-07-27 | Nippon Steel Corp | Catalyst for removing nitrogen oxide, and method and apparatus therefor |
-
1995
- 1995-09-26 CN CN95194720A patent/CN1071136C/en not_active Expired - Fee Related
- 1995-09-26 WO PCT/US1995/012339 patent/WO1996009891A1/en not_active Ceased
- 1995-09-26 AU AU36861/95A patent/AU3686195A/en not_active Abandoned
- 1995-09-26 CA CA002199373A patent/CA2199373A1/en not_active Abandoned
- 1995-09-26 MX MX9702145A patent/MX9702145A/en not_active IP Right Cessation
- 1995-09-26 EP EP95934553A patent/EP0783369A4/en not_active Withdrawn
-
1997
- 1997-03-24 NO NO971379A patent/NO971379D0/en not_active Application Discontinuation
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3029201A (en) * | 1959-12-28 | 1962-04-10 | Universal Oil Prod Co | Water treatment |
| US4028269A (en) * | 1975-08-21 | 1977-06-07 | Uop Inc. | Process for the preparation of a solid bed catalyst system |
| US4364843A (en) * | 1979-11-28 | 1982-12-21 | Uop Inc. | Catalytic composite, method of manufacture, and process for use |
Non-Patent Citations (1)
| Title |
|---|
| See also references of EP0783369A4 * |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005116169A1 (en) * | 2004-05-31 | 2005-12-08 | Agency For Science, Technology And Research | Novel process for removing sulfur from fuels |
| US8016999B2 (en) | 2004-05-31 | 2011-09-13 | Agency For Science, Technology And Research | Process for removing sulfur from fuels |
Also Published As
| Publication number | Publication date |
|---|---|
| AU3686195A (en) | 1996-04-19 |
| NO971379L (en) | 1997-03-24 |
| NO971379D0 (en) | 1997-03-24 |
| CA2199373A1 (en) | 1996-04-04 |
| EP0783369A4 (en) | 1998-12-09 |
| CN1071136C (en) | 2001-09-19 |
| EP0783369A1 (en) | 1997-07-16 |
| MX9702145A (en) | 1997-06-28 |
| CN1155853A (en) | 1997-07-30 |
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