Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Formaldehyde | HCID 712 | — |
| Edukt | Aniline | HCID 6115 | — |
| Edukt | 1-Methoxy-2-propanol | HCID 7900 | — |
| Produkt | Benzoxazines | HCID 17845026 | — |
Reaktionsschritte
The steps include: in a 2 L four-necked glass reactor equipped with a heating mantle, a temperature controller, an electric mixer and a condenser, 200 g of phenolic novolac resin (D) having high proportion of tetra-functional resin monomer and 124.5 g of paraformaldehyde are dissolved thoroughly in the presence of 816 g of a solvent propylene glycol monomethyl ether at 85° C., 169 g of aniline is dropped in the course of 3 hours into the reactor at constant speed by a quantitative pump to proceed the reaction at 85° C. After finishing the dropping addition of aniline, the temperature is kept at 85° C. for aging for 2 hours, then the temperature is raised to 105° C. After water and part of the solvent are removed, a benzoxazine resin solution with 56 wt % solid is obtained. According to gel permeation chromatography (GPC) analysis, the proportion of the tetra-functional resin monomer in this benzoxazine resin is up to 60 area percent (Area %) or more.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08536283B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-c3e5243daef94224812a8c25a84f46db |
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| Quellennotiz | uspto-grants-2013_09 |
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