CN1018735B - Preparation method of polybasic-alcohol fatty ester - Google Patents
Preparation method of polybasic-alcohol fatty esterInfo
- Publication number
- CN1018735B CN1018735B CN 88105350 CN88105350A CN1018735B CN 1018735 B CN1018735 B CN 1018735B CN 88105350 CN88105350 CN 88105350 CN 88105350 A CN88105350 A CN 88105350A CN 1018735 B CN1018735 B CN 1018735B
- Authority
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- China
- Prior art keywords
- accordance
- grease
- polyvalent alcohol
- reaction
- present
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
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- Lubricants (AREA)
- Fats And Perfumes (AREA)
Abstract
The present invention relates to a lubricating agent prepared from polyalcohol and grease by the reaction of ester exchange for the processing industry of polyvinyl chloride plastics. The present invention is polyalcohol fatty acid ester which is prepared from polyalcohol(glycerol or polyglycerine) and grease (animal grease or vegetable grease) under the protection of nitrogen and the catalysis of catalysts. The present invention has favorable quality of products, and the performance indexes reach the level of the similar foreign products. The present invention fills the blank of the type of inner lubricating agents in the processing industry of plastics in China.
Description
The present invention relates to a kind of preparation method of polyhydric alcohol fatty acid ester, belong to the industrial lubricant category of plastic working, particularly igelite processing industry with lubricator.
Adding lubricant in the plastic formula, is in order to improve resin flow when the forming process.Some resin such as polyvinyl chloride and ABS etc. must add lubricant in the course of processing, for polyvinyl chloride hard goods, all the more so especially.
Plastics with lubricator according to its mode of action, can be divided into external lubricant and internal lubricant two big classes.Internal lubricant can reduce the force of cohesion between polymer molecule, works effects such as quickening fusion, reduction melt viscosity, prolongation processing life-span, improve liquidity and improve the transparency.
Polyhydric alcohol fatty acid ester is a kind of plastic working industry internal lubricant commonly used.At present, domestic igelite processing industry.Mainly be to rely on this series products (as the Loxiol G16 of West Germany's Henkel (Henkel) company) of import to produce.
The processing condition of the Loxiol G16 product of West Germany's Henkel (Henkel) company are not reported.
Purpose of the present invention is to develop a kind of suitable internal lubricant for domestic igelite processing industry.
We have succeeded in developing the preparation method of polyhydric alcohol fatty acid ester.
Polyhydric alcohol fatty acid ester with method provided by the invention is made through probationary certificate, can reduce melt torque and melt temperature, promote plasticizing, shorten fusion time, improve the thermal shear stability of material, eliminate wall sticking phenomenon, except that significantly interior lubrication, and certain outer lubrication is arranged, and the material non-stick pan, color is normal, the Loxiol G16 of quality and West Germany's Henkel (Henkel) company is suitable, has reached purpose of the present invention.
The detection data are as follows:
The present invention realizes by following means:
A kind of industrial lubricant of plastic working that makes through transesterify by polyvalent alcohol and grease, the preparation method of polyhydric alcohol fatty acid ester.
Feature of the present invention is
Polyvalent alcohol adopts glycerine or Polyglycerine
Grease adopts animal grease or Vegetable oil lipoprotein
Reaction is omnidistance under nitrogen protection
Proportioning raw materials (weight ratio) is a polyvalent alcohol: grease=1: 3~5
Catalyzer adopts an alkali metal salt or metal catalyst
Reaction times is 5~12h
Temperature of reaction is 180~240 ℃.
It is characterized in that described animal grease is lard, tallow, suet or bone fat.
It is characterized in that described Vegetable oil lipoprotein is peanut oil, soya-bean oil or Viscotrol C.
It is characterized in that described optimum material proportion (weight ratio) is a polyvalent alcohol: grease=1: 2.5~4.
It is characterized in that described an alkali metal salt is oxyhydroxide, carbonate or the acid carbonate of sodium or potassium.
It is characterized in that described metal catalyst is an organotin 8831.
It is characterized in that described optimum reacting time is 7~10h
It is characterized in that described optimal reaction temperature is 200~230 ℃.
It is characterized in that its consumption of described catalyzer is 0.7~1.2% of the weight that feeds intake.
It is characterized in that described discoloring agent is aqueous hydrogen peroxide solution or carclazyte, its consumption is 0.1~0.5% of the weight that feeds intake.
Facts have proved that the present invention has finished the task of own proposition.
Below in conjunction with embodiment, the invention will be further described:
Example one: feed intake
Glycerine 1000g
Lard 3000g
Sodium hydroxide 28g
In the reactor that thermometer, condenser and agitator are housed, add above-mentioned material, logical nitrogen, heat to 180 ℃~240 ℃ under stirring, the reaction times is 5h, adds discoloring agent aqueous hydrogen peroxide solution 5.6ml, stirring down, decolouring is cooled to 110~130 ℃, filter, get product 3860g, productive rate 96.5%.Quality product: outward appearance light yellow transparent liquid, 0.925/20 ℃ of density, zero pour<0 ℃, 1.479/20 ℃ of refractive power, acid number 1, iodine number 65, viscosity 155MPa.S/50 ℃, 229 ℃ of flash-points, volatility 0.8%(96h/90 ℃), dimension card (Vicat) softening temperature is influenced 92, to the influence of transparency, transparent.
Example two: feed intake
Polyglycerine 1000g
Tallow, suet or bone fat 5000g
Yellow soda ash or sodium bicarbonate 72g
Carclazyte 30g
With example one equipment and operation, logical nitrogen.
Processing condition: 180 ℃~240 ℃ of interior temperature, time 12h gets product 5760g, productive rate 96%.Quality product: outward appearance light yellow transparent liquid, 0.930/20 ℃ of density, zero pour<0 ℃, 1.485/20 ℃ of refractive power, acid number 1.2, iodine number 80, viscosity 170MPa.S/50 ℃, 230 ℃ of flash-points, volatility 0.9%(96h/90 ℃), dimension card (Vicat) softening temperature is influenced 92, to the influence of transparency, transparent.
Example three: feed intake
Glycerine 1000g
Viscotrol C 2500g
Potassium hydroxide 24.5g
Aqueous hydrogen peroxide solution 9.8ml
With example one equipment and operation.
Processing condition: 200 ℃~230 ℃ of interior temperature, time 7h gets product 3377.5g, productive rate 96.5%.Quality product: outward appearance light yellow transparent liquid, 0.925/20 ℃ of density, zero pour<0 ℃, 1.481/20 ℃ of refractive power, acid number 1.3, iodine number 75, viscosity 169MPa.S/50 ℃, 230 ℃ of flash-points, volatility 0.85%(96h/90 ℃), dimension card (Vicat) softening temperature is influenced 92, to the influence of transparency, transparent.
Example four: feed intake
Polyglycerine 1000g
Peanut oil or soya-bean oil 4000g
Salt of wormwood or potassium bicarbonate 24.5g
Carclazyte 24g
With example one equipment and operation.
Processing condition: 200 ℃~230 ℃ of interior temperature, time 10h gets product 5760g, productive rate 96%.
Quality product: outward appearance light yellow transparent liquid, 0.930/20 ℃ of density, zero pour<0 ℃, 1.485/20 ℃ of refractive power, acid number 1.3, iodine number 70, viscosity 160MPa.S/50 ℃, 235 ℃ of flash-points, volatility 0.8%(96h/90 ℃).To the influence of dimension card (Vicat) softening temperature, 92, to the influence of transparency, transparent.
Example five:
Only catalyzer changes organotin 8831, and all the other are with example three, and the result is with example three.
Claims (10)
1, a kind of industrial lubricant of plastic working that makes through transesterify by polyvalent alcohol and grease, the preparation method of polyhydric alcohol fatty acid ester,
Feature of the present invention is
1.1 polyvalent alcohol adopts glycerine or Polyglycerine,
1.2 grease is animal grease or Vegetable oil lipoprotein;
1.3 reaction is omnidistance under nitrogen protection,
1.4 proportioning raw materials (weight ratio) is
Polyvalent alcohol: grease=1: 3~5,
1.5 adopt an alkali metal salt or metal catalyst,
1.6 the reaction times is 5~12h,
1.7 temperature of reaction is 180~240 ℃.
2, in accordance with the method for claim 1, it is characterized in that described animal grease is lard, tallow, suet or bone fat.
3, in accordance with the method for claim 1, it is characterized in that described Vegetable oil lipoprotein is peanut oil, soya-bean oil or Viscotrol C.
4, in accordance with the method for claim 1, it is characterized in that described optimum material proportion (weight ratio) is a polyvalent alcohol: grease=1: 2.5~4.
5, in accordance with the method for claim 1, it is characterized in that described an alkali metal salt is oxyhydroxide, carbonate or the acid carbonate of sodium or potassium.
6, in accordance with the method for claim 1, it is characterized in that described metal catalyst is an organotin 8831.
7, in accordance with the method for claim 1, it is characterized in that described optimum reacting time is 7~10h.
8, in accordance with the method for claim 1, it is characterized in that described optimal reaction temperature is 200~230 ℃.
9, in accordance with the method for claim 1, it is characterized in that its consumption of described catalyzer is 0.7~1.2% of the weight that feeds intake.
10, in accordance with the method for claim 1, it is characterized in that described discoloring agent is aqueous hydrogen peroxide solution or white scholar, its consumption is 0.1~0.5% of the weight that feeds intake.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN 88105350 CN1018735B (en) | 1988-10-11 | 1988-10-11 | Preparation method of polybasic-alcohol fatty ester |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN 88105350 CN1018735B (en) | 1988-10-11 | 1988-10-11 | Preparation method of polybasic-alcohol fatty ester |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1033834A CN1033834A (en) | 1989-07-12 |
CN1018735B true CN1018735B (en) | 1992-10-21 |
Family
ID=4833553
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN 88105350 Expired CN1018735B (en) | 1988-10-11 | 1988-10-11 | Preparation method of polybasic-alcohol fatty ester |
Country Status (1)
Country | Link |
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CN (1) | CN1018735B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1329175C (en) * | 2003-02-17 | 2007-08-01 | 深圳市海川实业股份有限公司 | Lubricant for processing polyvinyl chloride |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100485232C (en) * | 2003-08-08 | 2009-05-06 | 日产自动车株式会社 | Sliding member and production process thereof |
CN100424108C (en) * | 2006-04-13 | 2008-10-08 | 上海中科合臣股份有限公司 | Preparation method of plant oil polyalcohol |
CN101724491B (en) * | 2008-10-23 | 2012-11-14 | 中国石油化工股份有限公司 | Friction improver, preparation method and lubricating oil composition thereof |
CN101724492B (en) * | 2008-10-23 | 2012-12-12 | 中国石油化工股份有限公司 | Extreme pressure antiwear agent and preparation method thereof and lubricating oil combination |
CN103275812B (en) * | 2013-04-26 | 2014-12-10 | 青岛中科润美润滑材料技术有限公司 | Method for preparing base oil of lubricating oil from waste animal and vegetable oil |
-
1988
- 1988-10-11 CN CN 88105350 patent/CN1018735B/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1329175C (en) * | 2003-02-17 | 2007-08-01 | 深圳市海川实业股份有限公司 | Lubricant for processing polyvinyl chloride |
Also Published As
Publication number | Publication date |
---|---|
CN1033834A (en) | 1989-07-12 |
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