EP1561797A1 - Procédé d'amélioration d'huile - Google Patents
Procédé d'amélioration d'huile Download PDFInfo
- Publication number
- EP1561797A1 EP1561797A1 EP04250667A EP04250667A EP1561797A1 EP 1561797 A1 EP1561797 A1 EP 1561797A1 EP 04250667 A EP04250667 A EP 04250667A EP 04250667 A EP04250667 A EP 04250667A EP 1561797 A1 EP1561797 A1 EP 1561797A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- oil
- water
- acidic material
- added
- phase
- 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.)
- Withdrawn
Links
- 238000000034 method Methods 0.000 title claims abstract description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 25
- 239000000463 material Substances 0.000 claims abstract description 19
- 230000002378 acidificating effect Effects 0.000 claims abstract description 18
- 239000002699 waste material Substances 0.000 claims abstract description 15
- 239000000839 emulsion Substances 0.000 claims abstract description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims abstract description 5
- 235000011149 sulphuric acid Nutrition 0.000 claims abstract description 5
- 239000001117 sulphuric acid Substances 0.000 claims abstract description 5
- 238000004380 ashing Methods 0.000 claims abstract description 4
- 239000000126 substance Substances 0.000 claims abstract description 4
- 239000012071 phase Substances 0.000 claims description 16
- 239000008346 aqueous phase Substances 0.000 claims description 8
- 238000010438 heat treatment Methods 0.000 claims description 5
- 239000006185 dispersion Substances 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 3
- 238000005191 phase separation Methods 0.000 claims description 3
- 238000000926 separation method Methods 0.000 claims description 3
- 239000003518 caustics Substances 0.000 abstract description 6
- 239000000203 mixture Substances 0.000 abstract description 5
- 230000015572 biosynthetic process Effects 0.000 abstract description 4
- 238000004064 recycling Methods 0.000 abstract description 3
- 238000004945 emulsification Methods 0.000 abstract description 2
- 239000003921 oil Substances 0.000 description 38
- 239000002184 metal Substances 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 6
- 238000011109 contamination Methods 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000012855 volatile organic compound Substances 0.000 description 5
- 239000000356 contaminant Substances 0.000 description 4
- 239000000446 fuel Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000000295 fuel oil Substances 0.000 description 3
- 239000003513 alkali Substances 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 238000010924 continuous production Methods 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000010913 used oil Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000007857 degradation product Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000002737 fuel gas Substances 0.000 description 1
- 239000010763 heavy fuel oil Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 239000002910 solid waste Substances 0.000 description 1
- 230000003019 stabilising effect Effects 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M175/00—Working-up used lubricants to recover useful products ; Cleaning
- C10M175/005—Working-up used lubricants to recover useful products ; Cleaning using extraction processes; apparatus therefor
-
- 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
- C10G17/00—Refining of hydrocarbon oils in the absence of hydrogen, with acids, acid-forming compounds or acid-containing liquids, e.g. acid sludge
- C10G17/02—Refining of hydrocarbon oils in the absence of hydrogen, with acids, acid-forming compounds or acid-containing liquids, e.g. acid sludge with acids or acid-containing liquids, e.g. acid sludge
-
- 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
- C10G31/00—Refining of hydrocarbon oils, in the absence of hydrogen, by methods not otherwise provided for
- C10G31/08—Refining of hydrocarbon oils, in the absence of hydrogen, by methods not otherwise provided for by treating with water
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M175/00—Working-up used lubricants to recover useful products ; Cleaning
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M175/00—Working-up used lubricants to recover useful products ; Cleaning
- C10M175/0016—Working-up used lubricants to recover useful products ; Cleaning with the use of chemical agents
Definitions
- the present invention relates to a process and apparatus for the treatment of oils.
- the invention was developed in response to a need to purify waste oils to make them suitable for further use. Accordingly it has a particular relevance thereto, and will be more particularly described in that context. However, the treatment of other oils is not excluded from the compass of the invention.
- waste oils contain impurities and/or degradation products.
- Common impurities include particulate contamination, water, and original or degraded additives many of which contain metal atoms. Not only do these affect the combustion properties of the waste oil, but it is highly undesirable from the environmental point of view that oils with such levels of contamination should be burned. Accordingly, it is necessary to treat the waste oil to remove (or reduce) contaminants prior to their use as a fuel.
- waste oils can itself produce environmentally undesirable contamination, for example in the form of vapours of volatile organic compounds or VOCs, and in the form of metal containing by-products which are difficult to treat further (see below). Accordingly, any acceptable waste oil treatment must be arranged with these factors in mind.
- Water is commonly removed by treatment of the oils with a demulsifying agent (emulsion breaker), followed by separation as in a centrifuge for example.
- emulsion breaker demulsifying agent
- the present invention provides a method of oil treatment comprising the steps of treating the oil with water followed by treating the oil with an acidic material.
- the water is added in a manner such as to form a dispersion, and more preferably an emulsion, for example by injecting it ahead of a mixing device or pump such as a centrifugal pump.
- the water is added at a rate of at least 5% m/m (mass/mass), more preferably at least 10% and most preferably at least 13% m/m. Preferably it is added at a rate of no more than 20% m/m and more preferably no more than 17% m/m.
- the acidic material is subsequently injected so as to be dispersed in the oil, for example just ahead of a second mixing device or pump such as a second centrifugal pump.
- a preferred acidic material is inhibited concentrated sulphuric acid, e.g. 98% sulphuric acid.
- the acidic material is added at a rate of 500-10,000 ppm (parts per million m/m), more preferably 1,000 to 8,000 ppm and most preferably 2,000 to 7,000 ppm.
- the method according to the invention substantially avoids tar formation, or at least leads to a highly significant reduction in tar formation, thus providing a cleaner and more efficient oil treatment process.
- the mixture is preferably left for some time preferably at least 20 minutes, more preferably at least 40 minutes, and most preferably at least one hour, for reaction to occur, and preferably the mixture is stored in a holding tank for this period.
- a pipeline receiving the oil/water/acid mixture may be dimensioned according to the flow rate to permit the requisite residence time therein.
- a de-emulsifying and/or de-ashing chemical may be added, and the resulting phases separated, one of the separated phases being a purified oil phase.
- the latter may be further purified by being subjected to flash evaporation to provide a purified oil product in which relatively volatile VOCs and any remaining water are further reduced, but in many circumstances this is not expected to be necessary.
- the purified oil phase is treated with alkali, e.g. a caustic solution, to neutralise any residual acidity, which otherwise may prove unacceptably aggressive towards metal (for example during subsequent storage).
- alkali e.g. a caustic solution
- treatment of the separated aqueous phase with alkali such as a caustic solution is preferred to ensure that effluent from the process is not acidic.
- the oil is pretreated by heating and/or by phase separation before the water is added.
- Heating can serve to promote phase separation e.g. of an aqueous phase.
- the invention extends to apparatus arranged to perform the method.
- waste oil from a reservoir tank is initially passed through a heat exchanger 1 where it is warmed by heat exchange with the product 2 (exchanger 1 is shown at both ends of the process), and then subject to further heat input 3 if necessary.
- the heating process has the effect of de-watering the oil to a considerable extent, and accordingly the oil is then passed through a decanting centrifuge, where the separated oil and also some semi-solid waste products are removed as a stream 5.
- the treated oil 6 from centrifuge 4 is then filtered in an filter 7 to remove the bulk of the remaining solid or semi-solid contaminants.
- the filter 7 is enclosed to retain any VOC vapours.
- the centrifuge 4 would conventionally be enclosed so that vapour release is no problem there.
- the oil feed 8 output from filter 7 is then injected with water at a point 10 in a pipeline just prior to a first centrifugal pump (not shown), so that the water produces an emulsion 11.
- a first centrifugal pump not shown
- 98% sulphuric acid 13 is injected just ahead of a second centrifugal pump (not shown), and the mixture of materials is then allowed to stand in a first reaction vessel 14 for about one hour to allow reactions to proceed (alternatively in a continuous process a sufficiently large pipeline is used in lieu of vessel 14 to provide a residence time between its ends of about an hour).
- reaction product 15 in a pipeline from vessel 14 is then treated by injection with a de-ashing and de-emulsifying chemical 16 and then stored in a second reaction vessel 17 for around one hour to enable de-emulsification and other processes to proceed.
- the material 18 leaving the vessel 17 comprises a treated oil phase together with an aqueous phase and semisolid waste material. It is passed into a three-phase high speed centrifuge 19, which separates the aqueous phase 20 for purification and recycling to the water injection point 11, the semisolid waste 21 for disposal, and the treated oil phase 22.
- the treated oil phase 22 is amply clean enough for use as a fuel oil. Nevertheless, it may contain some residual acidity, and in a preferred arrangement the phase 22 is treated (not shown) with a caustic solution to neutralise this acidity. Furthermore, whether or not there is any preceding caustic treatment, the fuel oil phase 22 will commonly still contain some water and some relatively volatile VOCs, and at least in some circumstances this is undesirable. Therefore, as shown, as an optional additional stage, the treated oil phase 22 is passed into a flash vessel 25 where water and other relatively volatile materials 23 are removed for disposal, the purified treated oil phase 24 being passed through the heat exchanger 2 on its way to storage.
- the aqueous phase or at least that part being fed out as effluent, is also treated with caustic solution.
Landscapes
- 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)
- Combustion & Propulsion (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04250667A EP1561797A1 (fr) | 2004-02-07 | 2004-02-07 | Procédé d'amélioration d'huile |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04250667A EP1561797A1 (fr) | 2004-02-07 | 2004-02-07 | Procédé d'amélioration d'huile |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP1561797A1 true EP1561797A1 (fr) | 2005-08-10 |
Family
ID=34673737
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP04250667A Withdrawn EP1561797A1 (fr) | 2004-02-07 | 2004-02-07 | Procédé d'amélioration d'huile |
Country Status (1)
| Country | Link |
|---|---|
| EP (1) | EP1561797A1 (fr) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104698092A (zh) * | 2015-03-18 | 2015-06-10 | 中国石油大学(华东) | 一种净油累积转化率的评价方法 |
| WO2017024959A1 (fr) * | 2015-08-10 | 2017-02-16 | Shirhao Limited | Appareils et procédés de recyclage de substances fluidiques |
| WO2020162816A1 (fr) * | 2019-02-08 | 2020-08-13 | Skf Recondoil Ab | Procédé et système pour l'utilisation circulaire d'une huile industrielle |
| US11958004B2 (en) | 2019-02-08 | 2024-04-16 | Skf Recondoil Ab | Method and system for purification of contaminated oil |
| US12377367B2 (en) | 2020-05-18 | 2025-08-05 | Skf Recondoil Ab | Solvent extraction system and method |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB193029A (en) * | 1922-02-07 | 1924-01-10 | Apolline Rialland | Process for purifying mineral oils |
| US1686491A (en) * | 1927-01-19 | 1928-10-02 | Standard Oil Dev Co | Preparation of fuel oil |
| US2434528A (en) * | 1945-06-04 | 1948-01-13 | Standard Oil Dev Co | Method for removing ash-forming constituents and sediment from alkaline petroleum residuum |
| US2520407A (en) * | 1948-11-27 | 1950-08-29 | Sun Oil Co | Removal of inorganic matter from petroleum residua |
| US4491515A (en) * | 1981-03-23 | 1985-01-01 | Monash University | Treating used automotive lubricating oil to reduce the content of suspended particulate matter, including lead |
| WO1993013190A1 (fr) * | 1992-01-03 | 1993-07-08 | S & D Oil Technics B.V. | Procede d'extraction de polluants a partir d'huile usee |
| GB2393448A (en) * | 2002-09-28 | 2004-03-31 | Oss Group Ltd | Treatment of oil to reduce/prevent tar formation |
-
2004
- 2004-02-07 EP EP04250667A patent/EP1561797A1/fr not_active Withdrawn
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB193029A (en) * | 1922-02-07 | 1924-01-10 | Apolline Rialland | Process for purifying mineral oils |
| US1686491A (en) * | 1927-01-19 | 1928-10-02 | Standard Oil Dev Co | Preparation of fuel oil |
| US2434528A (en) * | 1945-06-04 | 1948-01-13 | Standard Oil Dev Co | Method for removing ash-forming constituents and sediment from alkaline petroleum residuum |
| US2520407A (en) * | 1948-11-27 | 1950-08-29 | Sun Oil Co | Removal of inorganic matter from petroleum residua |
| US4491515A (en) * | 1981-03-23 | 1985-01-01 | Monash University | Treating used automotive lubricating oil to reduce the content of suspended particulate matter, including lead |
| WO1993013190A1 (fr) * | 1992-01-03 | 1993-07-08 | S & D Oil Technics B.V. | Procede d'extraction de polluants a partir d'huile usee |
| GB2393448A (en) * | 2002-09-28 | 2004-03-31 | Oss Group Ltd | Treatment of oil to reduce/prevent tar formation |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104698092A (zh) * | 2015-03-18 | 2015-06-10 | 中国石油大学(华东) | 一种净油累积转化率的评价方法 |
| WO2017024959A1 (fr) * | 2015-08-10 | 2017-02-16 | Shirhao Limited | Appareils et procédés de recyclage de substances fluidiques |
| CN106422489A (zh) * | 2015-08-10 | 2017-02-22 | 顺豪有限公司 | 回收流体物质的装置与方法 |
| WO2020162816A1 (fr) * | 2019-02-08 | 2020-08-13 | Skf Recondoil Ab | Procédé et système pour l'utilisation circulaire d'une huile industrielle |
| CN113438966A (zh) * | 2019-02-08 | 2021-09-24 | 斯凯孚废油转化公司 | 用于工业油的循环使用的方法及系统 |
| US11958004B2 (en) | 2019-02-08 | 2024-04-16 | Skf Recondoil Ab | Method and system for purification of contaminated oil |
| US12097453B2 (en) | 2019-02-08 | 2024-09-24 | Skf Recondoil Ab | Method and system for circular use of industrial oil |
| AU2020217543B2 (en) * | 2019-02-08 | 2025-02-27 | Skf Recondoil Ab | A method and system for circular use of industrial oil |
| US12370477B2 (en) | 2019-02-08 | 2025-07-29 | Skf Recondoil Ab | Liquid composition for purification of oil |
| US12377367B2 (en) | 2020-05-18 | 2025-08-05 | Skf Recondoil Ab | Solvent extraction system and method |
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| AX | Request for extension of the european patent |
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| AKX | Designation fees paid | ||
| REG | Reference to a national code |
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| STAA | Information on the status of an ep patent application or granted ep patent |
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| 18D | Application deemed to be withdrawn |
Effective date: 20060213 |