Integrated fluid catalytic cracking and alkylation process
US-9434662-B2 · Sep 6, 2016 · US
US2016376510A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016376510-A1 |
| Application number | US-201615261003-A |
| Country | US |
| Kind code | A1 |
| Filing date | Sep 9, 2016 |
| Priority date | Mar 21, 2012 |
| Publication date | Dec 29, 2016 |
| Grant date | — |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
A method for producing a highly aromatic base oil of the present invention includes a step of hydrorefining a clarified oil to obtain a highly aromatic base oil having an aromatic content of 50% by mass or more determined by a column chromatography analysis method. The step of hydrorefining a clarified oil is preferably performed under conditions of a hydrogen pressure of 5.0 to 20.0 MPa, a temperature of 280 to 400° C., a hydrogen oil ratio of 300 to 750 NL/L, and a space velocity of 0.3 to 2.0 h −1 . According to the present invention, a highly aromatic base oil used for rubber processing, asphalt reclamation and the like, and a novel method for producing a highly aromatic base oil can be provided.
Opening claim text (preview).
1 . A method for producing a highly aromatic base oil comprising: hydrorefining a clarified oil to obtain a hydrorefined oil; and fractionation-treating and/or adsorption-treating the hydrorefined oil to obtain a highly aromatic base oil having an aromatic content of 50% by mass or more determined by a column chromatography analysis method, a content of benzo(a)pyrene of 1 ppm by mass or less, and a total content of the following aromatic compounds 1) to 8): 1) benzo(a)pyrene, 2) benzo(e)pyrene, 3) benzo(a)anthracene, 4) chrysene, 5) benzo(b)fluoranthene, 6) benzo(j)fluoranthene, 7) benzo(k)fluoranthene, and 8) dibenzo(a,h)anthracene of 10 ppm by mass or less. 2 . The method for producing a highly aromatic base oil according to claim 1 , wherein the hydrorefining the clarified oil is performed under conditions of a hydrogen pressure of 5.0 to 20.0 MPa, a temperature of 280 to 400° C., a hydrogen oil ratio of 300 to 750 NL/L, and a space velocity of 0.3 to 2.0 h −1 . 3 . A method for producing a mixed-base oil comprising: hydrorefining a clarified oil to obtain a hydrorefined oil; fractionation-treating and/or adsorption-treating the hydrorefined oil to obtain a highly aromatic base oil having an aromatic content of 50% by mass or more determined by a column chromatography analysis method, a content of benzo(a)pyrene of 1 ppm by mass or less, and a total content of the following aromatic compounds 1) to 8): 1) benzo(a)pyrene, 2) benzo(e)pyrene, 3) benzo(a)anthracene, 4) chrysene, 5) benzo(b)fluoranthene, 6) benzo(j)fluoranthene, 7) benzo(k)fluoranthene, and 8) dibenzo(a,h)anthracene of 10 ppm by mass or less; and mixing the highly aromatic base oil and one or more base oils selected from a mineral oil and a synthetic oil other than the highly aromatic base oil to obtain a mixed-base oil having an aromatic content of 50% by mass or more determined by a column chromatography analysis method, an aniline point of 100° C. or less, % C A of 20 to 80 according to ASTM D2140, a pour point of +10° C. or less, a glass-transition point of −30° C. to −60° C., a rate of aromatic carbon of 0.1 to 0.5, a content of benzo(a)pyrene of 1 ppm by mass or less, and a total content of the following aromatic compounds 1) to 8): 1) benzo(a)pyrene, 2) benzo(e)pyrene, 3) benzo(a)anthracene, 4) chrysene, 5) benzo(b)fluoranthene, 6) benzo(j)fluoranthene, 7) benzo(k)fluoranthene, and 8) dibenzo(a,h)anthracene of 10 ppm by mass or less. 4 . A highly aromatic base oil obtained by the producing method according to claim 1 , wherein the highly aromatic base oil has an aromatic content of 50% by mass or more determined by a column chromatography analysis method, an aniline point of 60° C. or less, % C A of 30 to 80 according to ASTM D2140, a pour point of +10° C. or less, a glass-transition point of −30° C. to −60° C., and a rate of aromatic carbon of 0.1 to 0.7. 5 . A mixed-base oil comprising the highly aromatic base oil according to claim 4 and one or more base oils selected from a mineral oil and a synthetic oil other than the highly aromatic base oil, wherein the mixed-base oil has an aromatic content of 50% by mass or more determined by a column chromatography analysis method, an aniline point of 100° C. or less, % C A of 20 to 80 according to ASTM D2140, a pour point of +10° C. or less, a glass-transition point of −30° C. to −60° C., and a rate of aromatic carbon of 0.1 to 0.5.
used as base material · CPC title
aromatic · CPC title
containing carbon, hydrogen and halogen only · CPC title
including a sorption process as the refining step in the absence of hydrogen · CPC title
Aromatics · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.