IP Library › Granted Patent US 8,597,502
Granted Patent B2
US 8,597,502 · App. 12/733,918 · Granted Dec 3, 2013

Method of manufacturing diesel fuel base stock and diesel fuel base stock thereof

Inventors: Yuichi Tanaka (Yokohama, JP); Kazuhito Sato (Kitakatsushika-gun, JP)
Assignees: Japan Oil, Gas and Metals National Corporation; Inpex Corporation; Nippon Oil Corporation; Japan Petroleum Exploration Co., Ltd.; Cosmo Oil Co., Ltd.; Nippon Steel Engineering Co., Ltd.
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,597,502
App. No.
12/733,918
Granted
Dec 3, 2013
Kind
B2
Abstract

Disclosed is a method of manufacturing a diesel fuel base stock improved in low-temperature flowability, including: fractionating in a first fractionator a synthetic oil obtained by Fisher-Tropsch synthesis into at least two fractions of a first middle fraction containing a component having a boiling range corresponding to diesel fuel oil, and a wax fraction containing a wax component heavier than the first middle fraction; hydroisomerizing the first middle fraction by bringing the first middle fraction into contact with a hydroisomerizing catalyst to produce a hydroisomerized middle fraction; hydrocracking the wax fraction by bringing the wax fraction into contact with a hydrocracking catalyst to produce a wax-decomposition component; and fractionating in a second fractionator a mixture of the produced hydroisomerized middle fraction and the produced wax-decomposition component, wherein rectification conditions in the first fractionator and/or rectification conditions in the second fractionator are adjusted to selectively reduce an n-paraffin having 19 or more carbon atoms in a heavy component contained in the diesel fuel base stock. Furthermore, disclosed is a diesel fuel base stock obtained by the manufacturing method.

Claims (13)

1. A method of manufacturing a diesel fuel base stock improved in low-temperature flowability, comprising:

(i) fractionating in a first fractionator a synthetic oil obtained by Fisher-Tropsch synthesis into at least two fractions of

a first middle fraction containing a component having a boiling range corresponding to diesel fuel oil and containing a light wax component of n-paraffins having 20 to 25 carbon atoms, and

a wax fraction containing a wax component heavier than the first middle fraction;

(ii) hydroisomerizing the first middle fraction by bringing the first middle fraction into contact with a hydroisomerizing catalyst to produce a hydroisomerized middle fraction;

(iii) hydrocracking the wax fraction by bringing the wax fraction into contact with a hydrocracking catalyst to produce a wax-decomposition component; and

(iv) fractionating in a second fractionator a mixture of the produced hydroisomerized middle fraction and the produced wax-decomposition component,

wherein rectification conditions in the first fractionator and/or rectification conditions in the second fractionator are adjusted to reduce the content of n-paraffin having 19 or more carbon atoms in a heavy component contained in the diesel fuel base stock, and

wherein the fractionation is conducted where the 90% by volume distillation temperature of the first middle fraction, which is a feedstock for the hydroisomerization, is higher than the 90% by volume distillation temperature of the diesel fuel base stock by 20° C. or more as one of the rectification conditions in the first fractionator.

2. The method of manufacturing a diesel fuel base stock according to claim 1 , wherein: the 90% by volume distillation temperature of the first middle fraction, which is a feedstock for the hydroisomerization, is 360° C. or higher, and the 90% by volume distillation temperature of the diesel fuel base stock is 340° C. or less.

3. The method of manufacturing a diesel fuel base stock according to claim 1 , wherein:

when bringing the first middle fraction into contact with the hydroisomerizing catalyst, the reaction temperature is 180° C. to 400° C., the hydrogen partial pressure is 0.5 MPa to 12 MPa, and the liquid hourly space velocity is 0.1 h −1 to 10.0 h −1 ; and,

when bringing the wax fraction into contact with the hydrocracking catalyst, the reaction temperature is 180° C. to 400° C., the hydrogen partial pressure is 0.5 MPa to 12 MPa, and the liquid hourly space velocity is 0.1 h −1 to 10.0 h −1 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 3, 2010
From: TANAKA, YUICHI; SATO, KAZUHITO
To: JAPAN OIL, GAS AND METALS NATIONAL CORPORATION; INPEX CORPORATION; NIPPON OIL CORPORATION; JAPAN PETROLEUM EXPLORATION CO., LTD.; COSMO OIL CO., LTD.; NIPPON STEEL ENGINEERING CO., LTD.
Reel/Frame 024330/0042 →
Priority Claims (1)
JP 2007-256544 · Sep 28, 2007 · national
Continuity (1)
Related Publication 20100294696A1 · Nov 25, 2010