Unlock instant, AI-driven research and patent intelligence for your innovation.

Anacardol ether acid and preparation method thereof

A technology of cardanol ether and cardanol, which is applied in the chemical field, can solve the problems of insufficient strength and high cost of alkyd resin, achieve the advantages of performance and environmental friendliness, reduce the cost of raw materials, and enhance the effect of application range

Inactive Publication Date: 2015-07-15
ANHUI MEIDONG BIOLOGICAL MATERIAL
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The object of the present invention is to provide a kind of cardanol ether acid, and described this cardanol ether acid will solve the technical problems of insufficient strength and high cost of alkyd resin in the prior art

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
  • Anacardol ether acid and preparation method thereof
  • Anacardol ether acid and preparation method thereof
  • Anacardol ether acid and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0025] Cardanol and chloroacetic acid are first used as raw materials to synthesize cardanol ether ethyl acid, and its specific synthesis is as follows: cardanol 195g (0.65mol) is added in a four-necked flask, solvent 95% ethanol is added, and sodium hydroxide (48g , 1.2mol) of 50% aqueous solution was slowly dropped into the system, the reaction was stirred at room temperature for 30min, then heated to reflux for 30min, then chloroacetic acid (122g, 1.3mol) was added dropwise to the system, and the reaction was continued to be heated to reflux for 60min , and then vacuum evaporated the excess ethanol in the system, then added hydrochloric acid (1M) to adjust the pH>2, added 300mL ethyl acetate to separate layers, washed the organic phase with distilled water three times, then dried with anhydrous sodium sulfate, filtered, filtered The cake was rinsed twice with ethyl acetate (60 mL), the obtained organic phases were combined and the solvent was evaporated to obtain a pale yell...

Embodiment 2

[0031] Add 222.987g of the compound fatty acid obtained in Experiment 1, 93g of glycerin into a four-necked flask, heat 45g of xylene to 150°C for esterification, and use a water separator to separate the water produced during the esterification process. When the theoretical water output is reached, cool down to 120°C. ℃, add phthalic anhydride (148g) in batches and reflux at 150-180℃ for 5 hours, after separating out the theoretical amount of water, continue heating, distill out xylene, monitor the viscosity and acid value, when the viscosity (xylene dilutes 50% ) at about 7200mPa.S, pH = 5 ~ 15, turn off the heating, when the temperature drops to 120 ° C, dilute with xylene to about 50%, and discharge to obtain alkyd resin.

[0032] The indicators of the 50% oily alkyd resin plus rare earth naphthenate and cobalt naphthenate catalyst are as follows:

[0033] Viscosity: 7200mPa.S, solid content: 58%, acid value: 8mgKOH / g

[0034] Surface dry: 22min, completely dry: 24h

[0...

Embodiment 3

[0037] First, cardanol and 3-chloropropionic acid were used as raw materials to synthesize cardanol ether ethyl acid. The specific synthesis was as follows: 195 g (0.65 mol) of cardanol was added to a four-necked flask, and 95% ethanol was added as a solvent, and then the hydrogen oxidized A 50% aqueous solution of sodium (48g, 1.2mol) was slowly dripped into the system, the reaction was stirred at room temperature for 30min, then heated to reflux for 30min, then 141.5g3-chloropropionic acid (1.3mol) was added dropwise to the system, the The reaction was continued to heat and reflux for 60 minutes, then the excess ethanol in the system was evaporated in vacuum, then hydrochloric acid (1M) was added to adjust the pH>2, 300mL ethyl acetate was added to separate layers, the organic phase was washed three times with distilled water, and then washed with anhydrous sodium sulfate After drying and filtering, the filter cake was rinsed twice with ethyl acetate (60 mL), the obtained org...

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
viscosityaaaaaaaaaa
acid valueaaaaaaaaaa
viscosityaaaaaaaaaa
Login to View More

Abstract

The invention provides anacardol ether acid which has a structural formula shown in the specification. The invention also provides a preparation method of the anacardol ether acid. The preparation method comprises the following steps: adding anacardol into a reaction vessel, adding an organic solvent to dissolve anacardol, then adding a metal hydroxide water solution into the reaction vessel, stirring, heating for refluxing, adding chlorinated fatty acid into the reaction vessel, heating for refluxing, carrying out vacuum distillation to remove excess organic solvent, adjusting pH to 1.5-3, adding ethyl acetate to layer, washing an organic phase by using distilled water, then drying by using anhydrous sodium sulfate, filtering to obtain a filter cake, rinsing the filter cake by using ethyl acetate, combining the organic phases, and removing the solvent by distillation to obtain paste solid, namely anacardol ether acid. According to the preparation method, the intermediate anacardol ether acid is synthesized by taking anacardol as a raw material, and then alkyd resin is synthesized by taking the intermediate anacardol ether acid as a raw material, so that not only is the cost of the raw materials reduced, but also the prepared alkyd resin has favorable performances in terms of heat resistance, hardness and the like.

Description

Technical field: [0001] The invention relates to the field of chemistry, in particular to polymer materials, in particular to intermediates for the preparation of alkyd resins, in particular to a cardanol ether acid and a preparation method. Background technique: [0002] Alkyd resins are oil-modified polyester resins formed by the condensation polymerization of polyols, phthalic anhydride and fatty acids or oils (fatty acid triglycerides). According to the number and structure of double bonds in fatty acid (or oil) molecules, it can be divided into three types: dry, semi-dry and non-dry. Drying alkyds cure in air; non-drying alkyds are mixed with amino resins and cured by heating. In addition, it can also be divided into alkyd resins with short, medium, long and very long oil degrees according to the content of fatty acid (or oil) or phthalic anhydride used. After the alkyd resin is cured to form a film, it is shiny and tough, has strong adhesion, and has good wear resist...

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 Patents(China)
IPC IPC(8): C07C59/68C07C59/70C07C51/367C08G63/668C08G63/676C08G63/49
CPCC07C51/367C07C59/68C07C59/70C08G63/48C08G63/676
Inventor 黎明黎炘宋学良
Owner ANHUI MEIDONG BIOLOGICAL MATERIAL