CN1074039C - Producing technology for refined jet fuel - Google Patents

Producing technology for refined jet fuel Download PDF

Info

Publication number
CN1074039C
CN1074039C CN97101474A CN97101474A CN1074039C CN 1074039 C CN1074039 C CN 1074039C CN 97101474 A CN97101474 A CN 97101474A CN 97101474 A CN97101474 A CN 97101474A CN 1074039 C CN1074039 C CN 1074039C
Authority
CN
China
Prior art keywords
reaction
tower
temperature
jet fuel
production process
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 - Fee Related
Application number
CN97101474A
Other languages
Chinese (zh)
Other versions
CN1194295A (en
Inventor
林运祥
张洪钧
邱继军
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
JINGMEN PETROCHEMICAL INST
Original Assignee
JINGMEN PETROCHEMICAL INST
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by JINGMEN PETROCHEMICAL INST filed Critical JINGMEN PETROCHEMICAL INST
Priority to CN97101474A priority Critical patent/CN1074039C/en
Publication of CN1194295A publication Critical patent/CN1194295A/en
Application granted granted Critical
Publication of CN1074039C publication Critical patent/CN1074039C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

The present invention discloses a production process for refined jet fuel, which relates to a method for decolouring and refining jet fuel. The production process adopts the common hydrofining to prepare a used catalyst. Raw materials are sent into a reaction tower by a pump, and react in the reaction tower. Then, reaction products are separated in a separate tower. After the reaction products are stripped by gas in a gas stripping tower, a finished product is prepared. The production process is characterized in that the reaction temperature in the reaction tower is from 40 to 180 DEG C. The production process has the advantages that jet fuel after being refined at low temperature has good color, moderate process conditions, small energy consumption and little reaction heat; when the production process is applied to industry, a reaction bed basically has no temperature rise.

Description

A kind of producing technology for refined jet fuel
The present invention relates to the method for decolorizing and refining of rocket engine fuel.
At present, China Guangzhou general petrochemicals factory of producer of hydrogenation method refined jet fuel, its hydrofining technology condition is: hydrogen dividing potential drop: 0.7-2.5MPa; Temperature (℃): 200-310; Hydrogen-oil ratio (V/V), 50-200:1; Volume space velocity (h -1): 1-8; Use common Hydrobon catalyst.When adopting the hydrogenation method refined jet fuel, general theory thinks that temperature is more than 200 ℃, and the hydrofining effect is relatively poor in the time of below 200 ℃.Its weak point is: temperature of reaction is had relatively high expectations, and has increased production cost.
Purpose of the present invention just provides a kind of production technique of refined jet fuel, and its technical process is simple, and temperature of reaction is lower, and it is good to face the rocket engine fuel color of hydrogen after refining, and energy consumption is little, reaction heat seldom, the reaction bed temperature rise after the industrialization is seldom.
A kind of producing technology for refined jet fuel, it adopts the smart employed catalyzer of general hydrogenation, raw material is squeezed into reaction tower through pump, in reaction tower, react, in knockout tower, separate then, be finished product after gas is carried in gas stripping column, it is characterized in that: raw material is selected the 2# rocket engine fuel for use, the base oil of 3# rocket engine fuel or 3# rocket engine fuel; Reaction conditions in reaction is taken is: temperature of reaction 40-180 ℃, the reactive hydrogen dividing potential drop is 0.7-2.5MPa, and hydrogen-oil ratio is 50-200:1 by volume, and volume space velocity is 1-8h -1Separation condition is in knockout tower: hydrogen pressure is 0.7-2.5MPa, and temperature is 40-180 ℃; Gas in gas stripping column is put forward condition: pressure 0.7-2.5MPa, temperature is 40-180 ℃.Said catalyzer is; Wi-W type or Wi-NO type Hydrobon catalyst.
The invention has the advantages that: the rocket engine fuel color behind the low-temperature purifying method is good, and processing condition relax, and energy consumption is little, and reaction heat seldom; During industrial application, reaction bed does not have temperature rise substantially.
Principle of work: with the RN-1 catalyzer is example, temperature when lesser temps≤80 ℃, and the R8-1 catalyzer mainly is to show as adsorption bleaching, and along with the increase of catalyzer absorption saturation ratio, its decolouring is active to descend, and it is shorter therefore to show as life of catalyst.Temperature is more than or equal to 120 ℃ when at comparatively high temps, and during smaller or equal to 180 ℃, this catalyzer trace impurity in the raw material such as colloid under facing the hydrogen state are removed by hydrogenation, a spot of unsaturated hydrocarbons by saturated as alkene etc., thereby improve the color of raw material, the decolouring activity that shows as catalyzer in its test-results is very stable, and the stability test of catalyzer is more than 2000 hours, during industrial application, life of catalyst is 1-3.Test-results sees attached list one.
Subordinate list one is character synopsis before and after the feed purification of the present invention
Base oil a part sieve essential oil with the 3# rocket engine fuel is a raw material, raw material is squeezed into reaction tower through pump, in reaction tower, react, in knockout tower, separate then, be finished product after gas is carried in gas stripping column, the reaction conditions in reaction tower is: temperature is 150 ℃, and the hydrogen dividing potential drop is 1.0MPa, volume space velocity is 5h-1, and hydrogen to oil volume ratio is 50: 1; Separation condition is in knockout tower, hydrogen pressure 0.7-2.5MPa, and temperature is 40-180 ℃; It is pressure 0.7-2.5MPa that gas in gas stripping column is put forward condition, and temperature is 40-180 ℃.Subordinate list one:
Project Molecular sieve essential oil raw material Refining back product
Total sulfur (PPa) content 35.2 34.8
Total nitrogen (PPa) content <1 <1
Iodine number (g iodine/100g) 0.6 0.24
Colloid (a/a) content 0.31% 0.24%
Aromatic hydrocarbons (a/a) content Monocycle 14.93% 14.70%
Dicyclo 0.64% 0.61%
Many rings 540PPa 524PPa
Total aromatic hydrocarbons (a/a) content 15.524% 15.362%
Color (number) +21 +28

Claims (1)

1, a kind of producing technology for refined jet fuel, it adopts the smart employed catalyzer of general hydrogenation, raw material is squeezed into reaction tower through pump, in reaction tower, react, in knockout tower, separate then, be finished product after gas is carried in gas stripping column, it is characterized in that: raw material is selected the 2# rocket engine fuel for use, the base oil of 3# rocket engine fuel or 3# rocket engine fuel; Reaction conditions in reaction is taken is: temperature of reaction 40-180 ℃, the reactive hydrogen dividing potential drop is 0.7-2.5MPa, and hydrogen-oil ratio is 50-200 by volume: 1, and volume space velocity is 1-8h -1Separation condition is in knockout tower: hydrogen pressure is 0.7-2.5MPa, and temperature is 40-180 ℃; It is pressure 0.7-2.5MPa that gas in gas stripping column is put forward condition, and temperature is 40-180 ℃.
CN97101474A 1997-03-24 1997-03-24 Producing technology for refined jet fuel Expired - Fee Related CN1074039C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN97101474A CN1074039C (en) 1997-03-24 1997-03-24 Producing technology for refined jet fuel

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN97101474A CN1074039C (en) 1997-03-24 1997-03-24 Producing technology for refined jet fuel

Publications (2)

Publication Number Publication Date
CN1194295A CN1194295A (en) 1998-09-30
CN1074039C true CN1074039C (en) 2001-10-31

Family

ID=5165763

Family Applications (1)

Application Number Title Priority Date Filing Date
CN97101474A Expired - Fee Related CN1074039C (en) 1997-03-24 1997-03-24 Producing technology for refined jet fuel

Country Status (1)

Country Link
CN (1) CN1074039C (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1061617A (en) * 1990-11-20 1992-06-03 杨家振 A kind of prescription of coal-tar type diesel and compound method
CN1110986A (en) * 1994-04-28 1995-11-01 湖南长泰能源实业有限公司 Prodn. technique and Equipment for epuration and prepn. of domestic fuel by utilizing carbon 5 cut
CN1138083A (en) * 1995-06-14 1996-12-18 中国石油化工总公司石油化工科学研究院 Method for production of light fuel and lubricating oil with high viscosity index

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1061617A (en) * 1990-11-20 1992-06-03 杨家振 A kind of prescription of coal-tar type diesel and compound method
CN1110986A (en) * 1994-04-28 1995-11-01 湖南长泰能源实业有限公司 Prodn. technique and Equipment for epuration and prepn. of domestic fuel by utilizing carbon 5 cut
CN1138083A (en) * 1995-06-14 1996-12-18 中国石油化工总公司石油化工科学研究院 Method for production of light fuel and lubricating oil with high viscosity index

Also Published As

Publication number Publication date
CN1194295A (en) 1998-09-30

Similar Documents

Publication Publication Date Title
CN103897731B (en) A kind of catalytic cracking diesel oil and C 10+the method of distillate mixture manufacturing light aromatics
CN101298566A (en) Method for preparing biocarbon solid acid catalyst and biodiesel
Sánchez et al. Value‐added products from fruit and vegetable wastes: a review
CN103289740A (en) Method for preparing clean fuel oil from coal tar
CN1057065C (en) Preparation of superhigh specific surface area active carbon
CN111978987B (en) Method for producing aviation kerosene by combining aviation kerosene, biomass oil and coal tar
US9637699B2 (en) Methods for processing nitrogen rich renewable feedstocks
CN101486926A (en) Method for preparing gasoline and diesel by oil washing hydrogenation
CN115678683A (en) Method for producing hydrogenated oil from waste oil
CN1074039C (en) Producing technology for refined jet fuel
CN101723788B (en) Separation method of cracking C5 fractions
CN111548450B (en) Hydrogenation method of high-chlorine C9 petroleum resin
CN101544537A (en) Method for producing low carbon chemical ethanol from C6 sugar alcohol
TWI266760B (en) Process for the preparation of propane-1,3-diol
CN102719319B (en) Method for preparing biological aviation fuel by utilizing cornus wilsoniana oil
KR102523485B1 (en) Method for producing bio-renewable propylene from oil and fat
CN1377869A (en) Process for producing purified dicyclic amylic diene and 5-sub ethyl-2-norbornene
CN112592737A (en) Method for producing low-freezing point biodiesel by coupling liquid catalysis with heterogeneous pour point depression
CN100503529C (en) Separation method for refining coarse piperyene
CN102320923B (en) Method for preparing dihydric alcohol by refining and separating dimethyl nylon acid
CN101209966A (en) Method for preparing dehydrolinalyl acetate from dehydrolinalool
CN1223515C (en) Method for preparing active carbon from caudex of sisal
WO2009054307A1 (en) Process for producing soft olefinic substance
CN210885867U (en) Special refining bed of ethylene refining plant deyne
CN112028729B (en) Method for catalytically isomerizing (+) -horn alkene from (+) -orange alkene-containing mixture

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C19 Lapse of patent right due to non-payment of the annual fee
CF01 Termination of patent right due to non-payment of annual fee