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Method for producing hydroisomerization catalyst and method for producing lubricant base oil

一种润滑油基础油、氢化异构的技术,应用在物理/化学过程催化剂、分子筛催化剂、化学仪器和方法等方向,能够解决制品收率限制、难高收率馏分、限定等问题,达到高异构化选择性的效果

Inactive Publication Date: 2015-02-04
JX NIPPON OIL & ENERGY CORP
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, this method has the following problems: the operating cost is high, the types of applicable raw oil are limited, and the product yield is limited by the type of raw oil, etc.
However, the above-mentioned catalysts used in catalytic dewaxing not only have isomerization ability but also have hydrocarbon cracking ability. Also proceeds, it is difficult to obtain the desired fraction in high yield

Method used

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  • Method for producing hydroisomerization catalyst and method for producing lubricant base oil
  • Method for producing hydroisomerization catalyst and method for producing lubricant base oil

Examples

Experimental program
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Effect test

manufacture example 1

[0093]

[0094] ZSM-22 zeolite composed of a crystalline aluminosilicate having a Si / Al ratio of 45 (hereinafter also referred to as "ZSM-22") was produced by hydrothermal synthesis in the following procedure.

[0095] First, the following four aqueous solutions were prepared.

[0096] Solution A: a solution obtained by dissolving 1.94 g of potassium hydroxide in 6.75 mL of ion-exchanged water.

[0097] Solution B: a solution in which 1.33 g of aluminum sulfate 18 hydrate was dissolved in 5 mL of ion-exchanged water.

[0098] Solution C: A solution obtained by diluting 4.18 g of 1,6-hexanediamine (organic template) with 32.5 mL of ion-exchanged water.

[0099] Solution D: a solution obtained by diluting 18 g of colloidal silica (Ludox AS-40 manufactured by Grace Davison) with 31 mL of ion-exchanged water.

[0100] Next, solution A was added to solution B, and stirred until the aluminum component was completely dissolved. After solution C was added to this mixed solution, ...

manufacture example 2

[0111]

[0112] A ZSM-48 type zeolite having an organic template and having a Si / Al ratio of 45 (hereinafter also referred to as "ZSM-48") was synthesized based on Applied Catalysis A: General vol. 299 (2006) 167-174.

[0113] First, prepare the following four reagents.

[0114] Reagent E: 2.97 g of sodium hydroxide.

[0115] Reagent F: 0.80 g of aluminum sulfate 18 hydrate.

[0116] Reagent G: 26.2 g of 1,6-hexanediamine (organic template).

[0117] Reagent H: 0.9ml of 98% sulfuric acid solution

[0118] Reagent 1: 75 g of colloidal silicon dioxide (Ludox AS-40 manufactured by Grace Davison Company) aqueous solution (SiO 2 Concentration is 40%).

[0119] Next, the above-mentioned reagents E, F, G, H, and I were added to 180 mg of ion-exchanged water, and stirred at room temperature for 2 hours to completely dissolve them.

[0120] The gel-like substance obtained by the above operations was transferred to a stainless steel autoclave reactor with an internal volume of 10...

manufacture example 3

[0125]

[0126] Based on the method described in JP2006-523136 A, SSZ-32 zeolite (hereinafter also referred to as "SSZ-32") was produced by hydrothermal synthesis in the following procedure.

[0127] Sodium hydroxide, aluminum sulfate, colloidal silicon dioxide, isobutylamine, and N-methyl-N'-isopropyl-imidazolium cations were mixed according to the following molar ratios.

[0128] SiO 2 / Al 2 o 3 =35,

[0129] The total amount of isobutylamine and N-methyl-N'-isopropyl-imidazolium cations is SiO 2 0.2 times of

[0130] The gel-like substance obtained by the above operations was transferred to a stainless steel autoclave reactor with an internal volume of 100 mL, and the autoclave reactor was rotated on a tumbling device at a speed of about 60 rpm in a furnace at 160° C. for 60 hours to perform hydrothermal treatment. synthesis reaction. After the reaction was completed, the reactor was cooled and opened, and dried overnight in a dryer at 60° C. to obtain SSZ-32 with a...

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Abstract

This method for producing a hydroisomerization catalyst is characterized by comprising: a first step, wherein a catalyst to be processed is prepared, said catalyst having a carrier, which contains a zeolite having a 10-membered ring one-dimensional porous structure, and at least one type of metal, which is carried by the carrier, selected from a group comprising a metal belonging to groups 8-10 in the periodic table, molybdenum and tungsten; and a second step, wherein the hydroisomerization catalyst, which has 0.4 to 2.5 mass% of carbon contained in a catalyst, is obtained by conducting a coking process on the catalyst to be processed using a carbon-containing compound.

Description

technical field [0001] The present invention relates to a hydroisomerization catalyst and a method for producing the same. Moreover, this invention relates to the manufacturing method of the lubricating oil base oil using a hydroisomerization catalyst. Background technique [0002] Among petroleum products, for example, lubricating oil, light oil, jet fuel, and the like are products that place emphasis on fluidity at low temperatures. Therefore, for base oils used in these products, it is desirable to completely or partially remove wax components such as normal paraffins and slightly branched isoparaffins, which are the cause of low-temperature fluidity reduction, or to convert them to other than wax components. ingredients. In recent years, hydrocarbons obtained by the Fischer-Tropsch synthesis method (hereinafter referred to as "FT synthetic oil") have attracted attention as raw material oils for the production of lubricating oils and fuels because they do not contain en...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J29/74B01J35/10C01B39/48C10G45/62C10G45/64
CPCB01J29/076C10G45/64B01J29/7884C10G45/62B01J29/7861B01J29/7892B01J29/78B01J29/703B01J2229/186B01J29/74B01J29/7461B01J29/7484B01J29/00B01J29/064B01J29/10B01J29/7092B01J29/7096C01B39/48B01J35/60C07C5/2791
Inventor 永易圭行早坂和章岩间真理绘
Owner JX NIPPON OIL & ENERGY CORP
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