Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Persulfate | HCID 24412 | — |
| Reactant | (2,2-dibromoethenyl)benzene | HCID 161726 | — |
| Reactant | Sodium Lauryl Sulfate | HCID 3423265 | — |
| Product | 2-Ethylhexanoic Acid | HCID 8697 | — |
Reaction Steps
A series of emulsion polymerizations of dibromostyrene (DBS)/2-ethylhexyl acrylate (2-EHA) were carried out in 8 oz. bottles. All the ingredients (122.50 or 180 parts by weight deionized water, 3 parts sodium dodecyl sulfate, 0.3 parts potassium persulfate, 0.2 parts t-dodecyl mercaptan and 100 parts total monomers in the ratio desired in the polymer) were charged into 8 oz. bottles and flushed well with nitrogen, and then reacted at 50° C. to about 45.8 or 36.5% solids in 15 hr. The whole bottle was cooled to room temperature and 3 parts deionized water and 0.18 parts 50% H2O2 added, followed by agitation for 20 minutes. The results of these preparations are set forth in Table I. The latices in Examples 1 and 2 perform well in a variety of coating applications, and display improved flame retardancy, while the latices in Examples 3 through 5 give very soft and tacky coatings.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05290636 |
|---|
| Source dataset | uspto-grants-1994_03 |
|---|
| ORD ID | ord-b9fbcf2b539a42e5adf884906811f80b |
|---|
| Source note | uspto-grants-1994_03 |
|---|