Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Melamine | HCID 7955 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Spiro[isobenzofuran-1(3H),9'-[9H]xanthen]-3-one, 2'-chloro-6'-(diethylamino)- | HCID 117320 | — |
| Solvent | Water | HCID 962 | — |
| Product | Melamine formaldehyde | HCID 93374 | — |
Reaction Steps
A solution prepared by dissolving 2.5 parts by weight of 3-diethylamino-7-chlorofluoran in 80 parts by weight of NISSEKI HISOL N-296 (an oil, a trade name, mfd. by Nippon Sekiyu Kagaku K.K.) was emulsified in 100 parts by weight of a 5% aqueous solution of pH 4.0 prepared by dissolving a styrene-maleic anhydride copolymer together with a small amount of sodium hydroxide. On the other hand, when a mixture of 10 parts by weight of melamine, 25 parts by weight of a 37% aqueous formaldehyde solution and 65 parts by weight of water was adjusted to pH 9.0 with sodium hydroxide and heated at 60° C., the mixture became transparent after 15 minutes and a melamine-formaldehyde precondensate was obtained. The precondensate was added to the emulsion obtained above, and the resulting mixture was continuously stirred for 4 hours while maintaining the mixture at 60° C., and then was cooled to room temperature. The solid content of the resulting microcapsule dispersion was 45%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07635662B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-9db1cb330c504d2d82f8b53c90754b23 |
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| Source note | uspto-grants-2009_12 |
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