Low-friction polymerizable composition

A polymer composition and low-friction technology, applied in lubricating compositions, base materials, petroleum industry, etc., can solve the problems of low processability and productivity, low heat resistance, high cost, etc., and achieve high heat resistance, Excellent processability, durability and reliability

Active Publication Date: 2019-09-17
LG CHEM LTD
View PDF21 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, PEEK is still unsuitable as components exposed to ultra-high pressure and ultra-high speed environments due to relatively low heat resistance, and PAI and PI are limited in application as components due to low processability and productivity and high cost.

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
  • Low-friction polymerizable composition
  • Low-friction polymerizable composition
  • Low-friction polymerizable composition

Examples

Experimental program
Comparison scheme
Effect test

preparation example 1

[0247] Preparation example 1. Synthesis of phthalonitrile compound (PN1)

[0248] The compound (PN1) of the following chemical formula A1 was synthesized as follows.

[0249] 32.7 g of a compound of the following chemical formula A2 and 120 g of DMF (dimethylformamide) were introduced into a 3-neck round bottom flask, and stirred at room temperature to dissolve. Subsequently, 51.9 g of the compound of the following chemical formula A3 was added, and 50 g of DMF was added, followed by stirring to dissolve. Subsequently, 62.2 g of potassium carbonate was introduced together with 50 g of DMF, and the temperature was raised to 85° C. while stirring. After reacting for about 5 hours, the solution was cooled to room temperature.

[0250] The cooled reaction solution was poured into a 0.2N aqueous hydrochloric acid solution to neutralize and precipitate it, and after filtration, it was washed with water. Thereafter, the filtered reactant was dried in a vacuum oven at 100° C. for...

preparation example 2

[0257] Preparation example 2. Synthesis of phthalonitrile compound (PN2)

[0258] The compound (PN2) of the following chemical formula A4 was synthesized as follows.

[0259] 28.0 g of 4,4'-bis(hydroxyphenyl)methane and 150 mL of DMF (dimethylformamide) were introduced into a 500 mL 3-necked round bottom flask, and stirred at room temperature to dissolve. Subsequently, 48.5 g of 4-nitrophthalonitrile was added, and 50 g of DMF was added, followed by stirring to dissolve. Subsequently, 58.1 g of potassium carbonate was introduced together with 50 g of DMF, and the temperature was raised to 85° C. while stirring. After reacting for about 5 hours, the solution was cooled to room temperature.

[0260] The cooled reaction solution was poured into a 0.2N aqueous hydrochloric acid solution to neutralize and precipitate it, and after filtration, it was washed with water. Thereafter, the filtered reactant was dried in a vacuum oven at 100° C. for one day, so that water and remaini...

preparation example 3

[0263] Preparation example 3. Synthesis of phthalonitrile compound (PN3)

[0264] The compound (PN3) of the following chemical formula A5 was synthesized as follows.

[0265] 160 g of a compound of the following chemical formula A6 and 200 g of DMF (dimethylformamide) were introduced into a 3-necked round bottom flask, and stirred at room temperature to dissolve. Subsequently, 52 g of the compound of the above chemical formula A3 was added, and 200 g of DMF was added, followed by stirring to dissolve. Subsequently, 62.2 g of potassium carbonate was introduced together with 100 g of DMF, and the temperature was raised to 85° C. while stirring. After reacting for about 5 hours, the solution was cooled to room temperature.

[0266] The cooled reaction solution was poured into 0.2N aqueous hydrochloric acid solution. Chloroform was added to the mixed solution to extract the product, and the extracted product was washed with water. Chloroform and the reaction solution DMF (di...

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

PropertyMeasurementUnit
decomposition temperatureaaaaaaaaaa
friction coefficientaaaaaaaaaa
friction coefficientaaaaaaaaaa
Login to view more

Abstract

The present invention relates to a low-friction polymerizable composition, a prepolymer thereof, and a material for a relative friction component using same. The low-friction polymerizable composition, according to the present invention, contains a curing agent and a filler in a pthalonitrile compound, thereby having high heat resistance, excellent processability, as well as excellent low-friction properties.

Description

technical field [0001] Cross References to Related Applications [0002] This application claims Korean Patent Application No. 10-2017-0061797 filed with KIPO on May 18, 2017 and Korean Patent Application No. 10-2018-0054368 filed with KIPO on May 11, 2018 rights and interests, the disclosure of which is incorporated herein by reference in its entirety. [0003] The present invention relates to a polymerizable composition having not only low friction characteristics but also excellent heat resistance, a prepolymer thereof, and an opposing friction component material using the same. Background technique [0004] In the automotive industry, many efforts are being made to reduce friction at energy transfer components (eg, power train, drive train, etc.) in order to reduce weight and improve energy efficiency. This is because only 15% of the energy of the fuel used in the car is transferred to the wheels, and 10% of this is lost due to friction of the drive components. [00...

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
Patent Type & Authority Applications(China)
IPC IPC(8): C08G73/10C08K5/3412C08K3/013C08L79/08
CPCC08K5/3412C08G73/10C08G77/388C08L79/08C08L83/08C08K3/013C08L2201/02C08G73/024C08G73/0253C08G73/026C08G73/0273C08G77/452C08G77/70C10M103/02C10M103/06C10M107/38C10M107/44C10M107/46C10M107/50C10M111/04C10M2201/0413C10M2201/0663C10M2213/0623C10M2217/0465C10M2221/0405C10M2229/0535C10N2040/02
Inventor 金相佑李承姬安起镐金尤利亚纳
Owner LG CHEM LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products