Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Itaconic acid | HCID 811 | — |
| Reactant | Vinylidene chloride | HCID 6366 | — |
| Reactant | tert-Butyl hydroperoxide | HCID 6410 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | Sodium Persulfate | HCID 62655 | — |
| Reactant | Sodium Pyrosulfite | HCID 656671 | — |
| Reactant | HCID 23687474 | HCID 23687474 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86755927 | HCID 86755927 | — |
Reaction Steps
8.75 g of Rhodacal™ A-246L and 875 g of deionized water were charged to a 3 liter three neck flask equipped with mechanical stirrer and dry ice-acetone condenser. The system was purged with nitrogen for 30 minutes. A monomer emulsion was obtained by mixing 455 g of distilled water, 8.75 g of Rhodacal™ A-246L, 70 g of ethyl acrylate, 14 g of itaconic acid, 616 g of vinylidene chloride and 13 g of 10% sodium persulfate with magnetic stirring. The reactor was immersed in a constant temperature bath at 35° C. 1.3 g of sodium persulfate, 2.6 g of sodium metabisulfite and 2 g of 1% ferrous sulfate were added to the reactor and then the monomer emulsion was pumped to the reactor over two hours. The latex was stirred one more hour and 1 ml each of t-butyl hydroperoxide(10%) and sodium formaldehyde bisulfite(10%) were added twice at 20 minute intervals and stirred one more hour. The latex was cooled and filtered. Glass transition temperature was 9° C. as measured by DSC, average particle size obtained from PCS was 60 nm and % solids was 32.3%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06130014 |
|---|
| Source dataset | uspto-grants-2000_10 |
|---|
| ORD ID | ord-c7907c70d2a24e0f8f96dc17a55f9bc5 |
|---|
| Source note | uspto-grants-2000_10 |
|---|