Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Process for producing pentaerythritol oleate

A technology of pentaerythritol oleate and pentaerythritol, which is applied in the field of preparation of pentaerythritol oleate, can solve the problems of poor catalyst reusability, affecting product appearance and performance, reducing yield and product purity, etc. Raw material cost, product color improvement effect

Inactive Publication Date: 2008-12-03
SUZHOU CHIEN SHIUNG INST OF TECH
View PDF1 Cites 7 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] 1. The use of acidic catalysts, especially sulfuric acid with strong corrosiveness and strong oxidizing properties, not only has a low reaction conversion rate, but also severely corrodes the equipment, and the removal of the catalyst requires subsequent processes such as neutralization and water washing, and the production line is long; at the same time, a large amount of waste water emissions will also pollute the environment
[0006] 2. The selectivity of the reaction is poor and there are many side reactions. Under acidic conditions, it is easy to generate by-products such as ether, sulfuric acid ester, and sulfur dioxide. When it is difficult to separate and purify the product, it also reduces the yield and the yield of the product. Purity, affecting the appearance and performance of the product, increasing the production cost
[0007] In addition, in the prior art, the catalyst can also be p-toluenesulfonic acid, p-aminobenzenesulfonic acid, metal oxides, etc. Although using these substances as a catalyst can overcome the above-mentioned several problems to a certain extent, there is a problem that the amount of catalyst used high reaction temperature, poor reusability of catalysts, etc.; and some catalysts remain in the product, which makes the product prone to qualitative change and poor product stability during storage

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Process for producing pentaerythritol oleate

Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0020] According to the preparation method of the pentaerythritol oleate of the present embodiment specifically comprises the steps:

[0021] (1). Pentaerythritol and excess oleic acid react under the catalysis of lanthanum methanesulfonate to obtain a light yellow liquid comprising product pentaerythritol oleate and excess raw material oleic acid:

[0022] Add 635.6 parts of oleic acid, 68.1 parts of pentaerythritol, 56.3 parts of toluene and 2.1 parts of lanthanum methanesulfonate into the esterification kettle, stir and heat the material to reflux under the protection of nitrogen, keep the temperature at 120-160°C, and after reflux for about 3 hours, Take a sample to measure the acid value. The reaction was stopped when the acid value was no longer significantly lowered. The catalyst is separated by filtration, and the filtered catalyst can be reused.

[0023] Wherein, the esterification reaction equation is:

[0024]

[0025] (2). The described light yellow liquid ob...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention relates to a method for preparing pentaerythritol oleic acid ester. The method comprises the following steps that: oleic acid and pentaerythritol generate esterification to produce the pentaerythritol oleic acid ester under the action of catalyst, wherein, the catalyst is lanthanum methanesulfonate. The preparation method has a simple technique, few side reactions, short production period, and high reaction yield and product purity, and can effectively reduce the production cost. Moreover, the aftertreatment is simple and the pollution on the environment is low.

Description

technical field [0001] The invention belongs to the technical field of synthesis of ester compounds in organic chemistry, in particular to a preparation method of pentaerythritol oleate. Background technique [0002] About 50% of lubricating oil enters the environment through volatilization and leakage during use, and the loss of hydraulic oil during use is as high as 70-80%. More than 95% of these lubricating oils are derived from petroleum, and the biodegradability of petroleum-based lubricating oils is very poor; on the other hand, the global oil resources are increasingly scarce, resulting in a shortage of petroleum-based lubricating oil resources. Therefore, the synthesis of biodegradable lubricant base oils from renewable resources has attracted extensive attention. [0003] Pentaerythritol oleate has excellent thermal stability and oxidation stability, good hydrolytic stability, excellent viscosity performance and low temperature performance, etc.; it not only has th...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): C07C69/58C07C67/08
Inventor 杜晓晗黄松鹤
Owner SUZHOU CHIEN SHIUNG INST OF TECH
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products