Soluble environment-friendly adhesive and preparation process thereof
A preparation process and adhesive technology, which are applied in the field of soluble environment-friendly adhesive and its preparation, can solve the problem of reducing the packing tightness of molecular chain segments, destroying the conjugated system of polymer molecular chains, poor dissolving ability of the adhesive, etc. To solve the problem of low bonding performance, improve bonding performance and improve bonding performance
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0033] The concrete preparation process of dihydroxybiphenyl polyamide is as follows:
[0034] Step 1: Dissolve 1kg of pyromellitic dianhydride in acetone, heat up to 70°C, add 0.48kg of absolute ethanol and 0.1kg of p-toluenesulfonic acid to it, and react under constant temperature reflux for 4-5h, and spin the obtained product Steamed, then washed with deionized water and saturated sodium chloride solution, and then dried in an oven at 50°C to obtain esterified terephthalic acid, because the two anhydride groups in pyromellitic dianhydride The group reacts with ethanol under the catalysis of p-toluenesulfonic acid to generate benzoate and benzoic acid groups;
[0035] Step 2: Add 1kg of the esterified terephthalic acid and acetone prepared in step 1 into the flask, raise the temperature to 80°C and reflux, at the same time add 1.1kg of thionyl chloride to the flask, reflux for 5 hours, and conduct the reaction on the obtained product solution Evaporation and crystallization...
Embodiment 2
[0038] The concrete preparation process of dihydroxybiphenyl polyamide is as follows:
[0039] Step 1: Dissolve 1 kg of pyromellitic dianhydride in acetone, heat up to 70°C, add 0.52 kg of absolute ethanol and 0.1 kg of p-toluenesulfonic acid to it, and react under constant temperature reflux for 4-5 hours, and spin the obtained product steamed, then washed with deionized water and saturated sodium chloride solution, and then dried in an oven at 50°C to obtain esterified terephthalic acid;
[0040] Step 2: Add 1kg of the esterified terephthalic acid and acetone prepared in step 1 into the flask, raise the temperature to 80°C for reflux, and simultaneously add 1.2kg of thionyl chloride to the flask, reflux for 5 hours, and conduct the reaction on the obtained product solution Evaporation and crystallization, and the obtained crystals are washed by absolute ethanol, and then dried in an oven at 50°C to obtain tetracarboxylic acid diester dichlorides. Due to the esterification of...
Embodiment 3
[0043] A preparation process of a soluble environment-friendly adhesive, the specific preparation process is as follows:
[0044] In the first step, 4 kg of the dihydroxybiphenyl polyamide prepared in Example 1 was added to the reaction kettle, and 8 kg of dimethylformamide and 0.4 kg of basic copper carbonate were added to it at the same time, and the temperature was raised to 100° C. to stir for 3 hours, and then Raise the temperature to 120°C for 2 hours, condense and collect the decomposed ethanol during the reaction, cool to room temperature after the reaction is complete, then filter, wash and dry with acetone to obtain dihydroxybiphenyl polyimide;
[0045] In the second step, 5kg of 3-hydroxy-2-pyridinecarboxylic acid was added to acetone, the temperature was raised to 80°C and refluxed, then 5.9kg of thionyl chloride was added to it, and the reaction was carried out under constant temperature reflux for 5 hours, and then 3-hydroxy-2 - picolinoyl chloride; add thionyl c...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com