IP Library Granted Patent US 9,476,006
Granted Patent B2
US 9,476,006 · App. 14/386,446 · Granted Oct 25, 2016

Highly aromatic base oil and method for producing highly aromatic base oil

Inventors: Yoshiyuki Morishima (Tokyo, JP); Takashi Ito (Tokyo, JP)
Assignee: JX NIPPON OIL & ENERGY CORPORATION
C10M105/06C10G45/68C10M105/52C10G2300/1048C10G2400/10C10G2400/30
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Quick Facts
Patent No.
US 9,476,006
App. No.
14/386,446
Granted
Oct 25, 2016
Kind
B2
Abstract

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.

Claims (83)

1. A method for producing a mixed-base oil comprising:

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; 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., and a rate of aromatic carbon of 0.1 to 0.5.

2. The method for producing a mixed-base oil according to claim 1 , wherein the mixed-base oil has 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.

3. A mixed-base oil comprising;

a highly aromatic base oil, obtained by a method comprising 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,

and having 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 kinematic viscosity at 40° C. of 100 mm 2 /s or more, a glass-transition point of −30° C. to −60° C., and a rate of aromatic carbon of 0.1 to 0.5;

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.

4. The mixed-base oil according to claim 3 , wherein the mixed-base oil has 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.

5. A method for producing a highly aromatic base oil comprising:

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, an aniline point of 60° C. or less, % C A of 30 to 80 according to ASTM D2140 a sour point of +10° C. or less, a kinematic viscosity at 40° C. of 100 mini/s or more, 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.

6. The method for producing a highly aromatic base oil according to claim 5 , wherein hydrorefining a clarified oil is performed under conditions of a hydrogen pressure of 10.0 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 .

7. A method for producing a mixed-base oil comprising:

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, an aniline point of 60° C. or less, 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.

8. A highly aromatic base oil, 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 kinematic viscosity at 40° C. of 100 mm 2 /s or more, 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.

9. A mixed-base oil comprising the highly aromatic base oil according to claim 8 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., 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.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 19, 2014
From: MORISHIMA, YOSHIYUKI; ITO, TAKASHI
To: JX NIPPON OIL & ENERGY CORPORATION
Reel/Frame 034210/0998 →
Priority Claims (2)
JP 2012-063978 · Mar 21, 2012 · national
JP 2012-208413 · Sep 21, 2012 · national
Continuity (1)
Related Publication 20150057205A1 · Feb 26, 2015