EP1260569A2 - Verfahren zur Herstellung eines nichtkrebserregenden, hocharomatischen Prozessöls - Google Patents

Verfahren zur Herstellung eines nichtkrebserregenden, hocharomatischen Prozessöls Download PDF

Info

Publication number
EP1260569A2
EP1260569A2 EP02076964A EP02076964A EP1260569A2 EP 1260569 A2 EP1260569 A2 EP 1260569A2 EP 02076964 A EP02076964 A EP 02076964A EP 02076964 A EP02076964 A EP 02076964A EP 1260569 A2 EP1260569 A2 EP 1260569A2
Authority
EP
European Patent Office
Prior art keywords
range
feed
distillate
extract
hydrotreating
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Withdrawn
Application number
EP02076964A
Other languages
English (en)
French (fr)
Other versions
EP1260569A3 (de
Inventor
Yajnanarayana Halmuthur Jois
Krishna Rangraj Kaushik
Abraham Robert De Kraker
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.)
Shell Internationale Research Maatschappij BV
Original Assignee
Shell Internationale Research Maatschappij BV
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 Shell Internationale Research Maatschappij BV filed Critical Shell Internationale Research Maatschappij BV
Publication of EP1260569A2 publication Critical patent/EP1260569A2/de
Publication of EP1260569A3 publication Critical patent/EP1260569A3/de
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G45/00Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G2400/00Products obtained by processes covered by groups C10G9/00 - C10G69/14
    • C10G2400/10Lubricating oil

Definitions

  • the invention is related to a process for obtaining non-carcinogenic aromatic oils from a mixed distillate and an extract feed obtained in the manufacture of lubricant base oils.
  • a simple feed blending and hydrotreating process is shown for producing aromatic process oil, which shows a mutogenicity index of less than one by a Modified Ames Test.
  • Repsol Petroleo patent EP-839891 discloses a process for obtaining aromatic oils with a polycyclic aromatic compounds content of less than 3% (IP-346) from the mixed extract flow obtained in the manufacture of lubricant base oils, a flow which contains a polar solvent, preferably phenol, furfural or N-methyl-2-pyrrolidone (NMP), especially furfural, comprises: (a) cooling the flow of mixed extract to render non-polyaromatic components insoluble; (b) settling to bring about separation of the phases; (c) total or partial redissolution in solvent of the light phase obtained from the settling in (b); (d) cooling to effect separation of the non-polyaromatic components; and (e) settling to recover the light phase having a low polyaromatic compounds (PCA) content.
  • a polar solvent preferably phenol, furfural or N-methyl-2-pyrrolidone (NMP), especially furfural
  • Extract from the lubes extraction unit is re-extracted by another column (via countercurrent extraction methodology) at low temperatures.
  • the major advantage for this process seems to be that it is a single step process.
  • investment costs for a separate countercurrent extractor devoted to a high polycyclic stream is expensive.
  • Using an existing lube extractor for this process might lead to other product contamination with PCA.
  • US-A-3619414 is different from Applicants' process.
  • the feed of this process is a "petroleum distillate" and the process is used for improving electrical properties or for obtaining a lighter color.
  • the process describes approximately 30% aromatics in the product.
  • US-A-3462358 discloses hydrorefining of the distillates and the product is used for electrical applications.
  • the art of hydrorefining of the distillates is different from hydrotreating.
  • An atmospheric distillate or a vacuum distillate stream is combined with a lubricant extract stream.
  • a known quantity, i.e., ratio, of distillate and lubricant extract streams are blended in a mixer/feed tank.
  • This well-mixed stream is then hydrotreated to obtain a product having a desired aromatic content, i.e., non-carcinogenic, high aromatic process oil.
  • This process has more operating flexibility, yield and better efficiency than the processes reported in the prior literature.
  • desired levels of high aromatic lubricant streams and the desired solvency properties can be achieved by varying the ratio of the feed stream components and hydrotreating conditions.
  • pole oil is used as a carrier for pentachlorophenol (an insecticide) to treat wood (as a preservative).
  • pentachlorophenol an insecticide
  • development of a non-carcinogenic pole treating oil is a challenging area due to the properties required (a high aromatic, low viscosity stream with a flash point above 150 °F).
  • AWPA American Wood Preservative Association
  • the lube extract stream is the fraction as obtained when removing aromatics by means of solvent extraction from a petroleum fraction boiling in the lubricating oil range.
  • Such extraction processes are known to be used in a process to prepare a lubricating base oil.
  • the petroleum fraction boiling in the lubricating base oil range is suitably obtained by first distilling a crude petroleum feedstock at atmospheric pressure and subsequently performing a vacuum distillation on the residue of the atmospheric distillation.
  • the distillate products obtained in the vacuum distillation also referred to as vacuum distillates, are the petroleum fractions boiling in the lubricating base oil range.
  • Solvent refining and hydrorefining are process steps to prepare a base oil product starting from the petroleum fractions boiling in the lubricating base oil range as for example described in Lubricant base oil and wax processing, Avilino Sequeira, Jr., Marcel Dekker Inc., New York, 1994, pages 2-4.
  • the boiling range of the vacuum distillates are suitably between 300 and 620 °C and preferably between 350 and 580 °C.
  • Deasphalted residues of the above mentioned vacuum distillation are also considered to be the petroleum fractions boiling in the lubricating base oil range according to this invention.
  • hydrotreater After the two streams are well mixed, the resulting mixture is fed into a hydrotreater where it is processed under predetermined conditions, as is also well known to those skilled in the art as for example described in Lubricant base oil and wax processing, Avilino Sequeira, Jr., Marcel Dekker Inc., New York, 1994, pages 138-147.
  • suitable hydrotreating catalyst could be selected from the group of Nickel-Molybdenum and Nickel-Cobalt catalysts.
  • Typical operating conditions of the hydrotreating process are pressures in the range of 2.72-20.4 Mpa (400-3000 psi), preferably between 6.12 and 8.16 Mpa (900 and 1200 psi) and temperatures in the range of 204-427 °C (400-800 °F) and preferably between 265 and 321 °C (510 and 610 °F).
  • the resulting process oil exits the hydrotreater having the desired characteristics of high aromaticity and being non-carcinogenic.
  • Feed 1 in Table 2 Distillate extracts (25 wt%) and a distillate (75 wt%) were mixed well by stirring at 50 °C for one hour. The sample was drawn out and its properties were measured: Density 0.9120 g/cc at 15.5 °C (60 °F) and the other feed properties are listed in Table 2 for Feed 1.
  • Feed 2 in Table 2 Distillate extracts (20 wt%) and a distillate (80 wt%) were mixed well by stirring at 50 °C for one hour. The sample was drawn out and its properties were measured: Density 0.9046 g/cc at 15.5 °C (60 °F); D2887E Distillation 5% 411, 50% 509, 95% 939 °F; and the other feed properties are listed in Table 2 for Feed 2.
  • the feed (as detailed in Example 2 above) was used.
  • the feed was hydrotreated in a hydrotreating unit using a typical Ni-Mo lube oil hydrotreating catalyst at a liquid hourly space velocity (LHSV) of 0.5, at 288 °C (550 °F) and at 6.8 Mpa (1000 psi) hydrogen pressure.
  • LHSV liquid hourly space velocity
  • the unit was allowed to line-out for several hours before collecting the product.
  • the product has density 0.91 g/cc at 15.5 °C (60 °F); D2887E Distillation 5% 228 °C (443), 50% 283 °C (542), 95% 505 °C (942 °F); Kinematic viscosity 10.3 cSt at 40 °C, 2.43 cSt at 100 °C; Minimum of 10% pentachlorophenol solubility; Pour Point -57 °C (-70 °C); Color L4.5; D2549: Saturates 62.84%, Aromatics 36.32%, Polars 0.84%.
  • Table 3 The other properties of the product are listed in Table 3.
  • Example 4 was repeated using Feed 3. The results are in Table 4.
  • UV Aromatics is a standard UV spectrophotometric method wherein an aromatic type in lubricant base oils is measured. Using this method one could measure the amount of benzenes (mono-aromatics), naphthalenes (diaromatic), phenanthrenes (triaromatics), chrysenes, tetraphenes, and polyaromatics in mmol/100 gram of oil sample. A slight increase in the aromaticity relative to feed could be due to a change in molecular weight.

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)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
  • Lubricants (AREA)
EP02076964A 2001-05-21 2002-05-21 Verfahren zur Herstellung eines nichtkrebserregenden, hocharomatischen Prozessöls Withdrawn EP1260569A3 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US09/862,794 US20030168382A1 (en) 2001-05-21 2001-05-21 Process for making non-carcinogentic, high aromatic process oil
US862794 2001-05-21

Publications (2)

Publication Number Publication Date
EP1260569A2 true EP1260569A2 (de) 2002-11-27
EP1260569A3 EP1260569A3 (de) 2003-11-05

Family

ID=25339372

Family Applications (1)

Application Number Title Priority Date Filing Date
EP02076964A Withdrawn EP1260569A3 (de) 2001-05-21 2002-05-21 Verfahren zur Herstellung eines nichtkrebserregenden, hocharomatischen Prozessöls

Country Status (2)

Country Link
US (1) US20030168382A1 (de)
EP (1) EP1260569A3 (de)

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009126974A2 (en) * 2008-04-10 2009-10-15 Shell Oil Company Diluents, method for preparing a diluted hydrocarbon composition, and diluted hydrocarbon compositions
CN102311784A (zh) * 2010-07-07 2012-01-11 中国石油化工股份有限公司 一种环保芳烃油的生产方法
RU2450045C1 (ru) * 2010-09-29 2012-05-10 Общество с ограниченной ответственностью "Инпрогресс" Способ получения базовых масел с низким содержанием серы и экологически чистых ароматических наполнителей и пластификаторов каучука и резины
US8450538B2 (en) 2008-04-10 2013-05-28 Shell Oil Company Hydrocarbon composition
CN104593063A (zh) * 2013-11-04 2015-05-06 中国石油化工股份有限公司 一种中低温煤焦油生产橡胶填充油基础油的方法
CN104593065A (zh) * 2013-11-04 2015-05-06 中国石油化工股份有限公司 一种环保型橡胶填充油的生产方法
CN104593066A (zh) * 2013-11-04 2015-05-06 中国石油化工股份有限公司 中低温煤焦油生产环保型橡胶填充油的方法
CN104910953A (zh) * 2015-06-01 2015-09-16 中国石化集团金陵石油化工有限责任公司 一种脱除重质油品中稠环芳烃组分的工艺
CN105838419A (zh) * 2015-01-12 2016-08-10 中国石油化工股份有限公司 一种芳烃橡胶油的制备方法
CN106675647A (zh) * 2015-08-19 2017-05-17 中国石化扬子石油化工有限公司 一种环保填充油的制备方法
CN111087016A (zh) * 2018-10-24 2020-05-01 中国石油化工股份有限公司 粗四氯化钛除钒方法
US11332679B2 (en) 2015-05-12 2022-05-17 Ergon, Inc. High performance process oil
EP4092097A1 (de) * 2015-05-12 2022-11-23 Ergon, Inc. Hochleistungsprozessöl auf basis von destillierten aromatischen extrakten

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1967571A1 (de) * 2007-02-21 2008-09-10 BP p.l.c. Zusammensetzungen und Verfahren

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3303125A (en) * 1963-12-12 1967-02-07 Exxon Standard Sa Preparation of oils of high solvent character
US3997430A (en) * 1973-03-29 1976-12-14 Gulf Research & Development Company Hydrodesulfurization process involving blending high boiling streams
US5275990A (en) * 1991-10-31 1994-01-04 Amoco Corporation Process for regenerating a spent resid hydroprocessing catalyst using a group IIA metal
US6171477B1 (en) * 1997-06-10 2001-01-09 Institut Francais Du Petrole Hydroconversion of vacuum distillates and deasphalted oils in fixed beds and boiling beds

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3303125A (en) * 1963-12-12 1967-02-07 Exxon Standard Sa Preparation of oils of high solvent character
US3997430A (en) * 1973-03-29 1976-12-14 Gulf Research & Development Company Hydrodesulfurization process involving blending high boiling streams
US5275990A (en) * 1991-10-31 1994-01-04 Amoco Corporation Process for regenerating a spent resid hydroprocessing catalyst using a group IIA metal
US6171477B1 (en) * 1997-06-10 2001-01-09 Institut Francais Du Petrole Hydroconversion of vacuum distillates and deasphalted oils in fixed beds and boiling beds

Cited By (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009126974A2 (en) * 2008-04-10 2009-10-15 Shell Oil Company Diluents, method for preparing a diluted hydrocarbon composition, and diluted hydrocarbon compositions
WO2009126974A3 (en) * 2008-04-10 2010-03-18 Shell Oil Company Method for preparing a diluted hydrocarbon composition, and diluted hydrocarbon compositions
US8450538B2 (en) 2008-04-10 2013-05-28 Shell Oil Company Hydrocarbon composition
US8734634B2 (en) 2008-04-10 2014-05-27 Shell Oil Company Method for producing a crude product, method for preparing a diluted hydrocarbon composition, crude products, diluents and uses of such crude products and diluents
CN102311784A (zh) * 2010-07-07 2012-01-11 中国石油化工股份有限公司 一种环保芳烃油的生产方法
RU2450045C1 (ru) * 2010-09-29 2012-05-10 Общество с ограниченной ответственностью "Инпрогресс" Способ получения базовых масел с низким содержанием серы и экологически чистых ароматических наполнителей и пластификаторов каучука и резины
CN104593066B (zh) * 2013-11-04 2016-03-02 中国石油化工股份有限公司 中低温煤焦油生产环保型橡胶填充油的方法
CN104593065B (zh) * 2013-11-04 2016-03-30 中国石油化工股份有限公司 一种环保型橡胶填充油的生产方法
CN104593066A (zh) * 2013-11-04 2015-05-06 中国石油化工股份有限公司 中低温煤焦油生产环保型橡胶填充油的方法
CN104593065A (zh) * 2013-11-04 2015-05-06 中国石油化工股份有限公司 一种环保型橡胶填充油的生产方法
CN104593063A (zh) * 2013-11-04 2015-05-06 中国石油化工股份有限公司 一种中低温煤焦油生产橡胶填充油基础油的方法
CN104593063B (zh) * 2013-11-04 2016-03-30 中国石油化工股份有限公司 一种中低温煤焦油生产橡胶填充油基础油的方法
CN105838419A (zh) * 2015-01-12 2016-08-10 中国石油化工股份有限公司 一种芳烃橡胶油的制备方法
CN105838419B (zh) * 2015-01-12 2017-11-03 中国石油化工股份有限公司 一种芳烃橡胶油的制备方法
US11332679B2 (en) 2015-05-12 2022-05-17 Ergon, Inc. High performance process oil
US20220275292A1 (en) * 2015-05-12 2022-09-01 Ergon, Inc. High performance process oil
EP4092097A1 (de) * 2015-05-12 2022-11-23 Ergon, Inc. Hochleistungsprozessöl auf basis von destillierten aromatischen extrakten
US11560521B2 (en) 2015-05-12 2023-01-24 Ergon, Inc. High performance process oil
US11566187B2 (en) * 2015-05-12 2023-01-31 Ergon, Inc. High performance process oil based on distilled aromatic extracts
CN104910953A (zh) * 2015-06-01 2015-09-16 中国石化集团金陵石油化工有限责任公司 一种脱除重质油品中稠环芳烃组分的工艺
CN106675647A (zh) * 2015-08-19 2017-05-17 中国石化扬子石油化工有限公司 一种环保填充油的制备方法
CN111087016A (zh) * 2018-10-24 2020-05-01 中国石油化工股份有限公司 粗四氯化钛除钒方法

Also Published As

Publication number Publication date
EP1260569A3 (de) 2003-11-05
US20030168382A1 (en) 2003-09-11

Similar Documents

Publication Publication Date Title
JP5192136B2 (ja) ゴム用プロセスオイル
KR101465311B1 (ko) 공정유, 탈아스팔트유의 제조 방법, 추출물의 제조 방법, 및 공정유의 제조 방법
AU662115B2 (en) Non-carcinogenic bright stock extracts and deasphalted oils and process for the production thereof
EP1260569A2 (de) Verfahren zur Herstellung eines nichtkrebserregenden, hocharomatischen Prozessöls
JPH06116571A (ja) 高粘度指数低粘度潤滑油基油の製造法
US5840175A (en) Process oils and manufacturing process for such using aromatic enrichment with extraction followed by single stage hydrofinishing
EP0458574A2 (de) Verfahren zur Erzeugung von Transformatoröl aus hydrogekracktem Material
US5846405A (en) Process oils and manufacturing process for such using aromatic enrichment and two pass hydrofinishing
CN110607191B (zh) 渣油加氢处理和光亮油生产组合工艺
EP0892032B1 (de) Verfahren zur Herstellung der Produktölen mit Aromaten-anreichung und Zweistüfen- Hydrorraffinierung
US3992283A (en) Hydrocracking process for the maximization of an improved viscosity lube oil
CA1093490A (en) Process for the production of lubricating oils from sulfur-containing petroleum stocks
EP1272591B1 (de) Verfahren zur fabrikation von prozessölen
US3481863A (en) Refining high sulfur lubricating oil charge stocks
CN110105773B (zh) 一种环保型烷烃橡胶油及其制备方法
CN112251256B (zh) 渣油加氢处理和光亮油以及芳香基矿物油生产组合工艺
US3663427A (en) Preparation of lube hydrocracking stocks
CN114437816B (zh) 润滑油基础油和芳香基矿物油的组合生产方法和装置
SU757588A1 (ru) Способ получения электроизоляционного масла
CA2311077A1 (en) An improved method for making a process oil by using aromatic enrichment with extraction followed by single stage hydrofinishing
EP0238740B1 (de) Verfahren zur Verbesserung der Herstellung von Brightstock
WO1997009291A1 (en) Addition of co-solvents to furfural for aromatic extractions
EP1164181A1 (de) Erzeugung von Prozessölen
JPH0350366B2 (de)
JPH03197594A (ja) 潤滑油基油およびその製造方法

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR

AX Request for extension of the european patent

Free format text: AL;LT;LV;MK;RO;SI

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Kind code of ref document: A3

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR

AX Request for extension of the european patent

Extension state: AL LT LV MK RO SI

17P Request for examination filed

Effective date: 20040322

AKX Designation fees paid

Designated state(s): DE FR GB IT NL SE

17Q First examination report despatched

Effective date: 20041216

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20050427