Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acrylic Acid | HCID 6581 | — |
| Reactant | Butyl Methacrylate | HCID 7354 | — |
| Reactant | Styrene | HCID 7501 | — |
| Reactant | 2,4,4-Trimethyl-1-pentene | HCID 7868 | — |
| Reactant | Butyl Acrylate | HCID 8846 | — |
| Reactant | 2-Propenoic acid, 3-hydroxypropyl ester | HCID 33101 | — |
| Solvent | Butyl Acetate | HCID 31272 | — |
| Product | HCID 131724291 | HCID 131724291 | — |
Reaction Steps
Charge 1 was added to a 4-liter stirred stainless steel pressure reactor. The reactor was then pressurized with nitrogen providing a 5 psig pad on the reactor. The agitation on the reactor was set and the reactor temperature was adjusted to 150° C. Charge 2 was added to the reactor at addition rate of 52 grams/hour over 2.5 hours. After 15 minutes Charge 3 was added to reactor at the addition rate 500 grams/hour over 2 hours. During the monomer addition the temperature was maintained at 150° C. at 100 PSI. After charge 2 and charge 3 were in the reactor, the reaction mixture was held for 2 hours. The reactor was then cooled to 25° C., and vented. GC analysis of the reaction mixture showed that all acrylates, methacrylates and styrene were reacted. The reaction mixture was transferred to a 3 L flask, and was vacuum-stripped at 130° C. The final solids of the resulting polymer was determined by adding 200 grams of butyl acetate to the polymer mixture. The solids were measured at 82.2% at 110° C. for one hour. The copolymer had Mn=1560 and Mw/Mn=2.2. The 13C NMR spectrum is consistent with a molar copolymer composition of 20.4% Diisobutylene, 36.3% Hydroxypropyl acrylate, 16.1% Butyl methacrylate, 8.1% Styrene, 2.4% Acrylic acid, and 17.6% Butyl acrylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07132476B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-2dcb199cb141440594742bb66484f02d |
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| Source note | uspto-grants-2006_11 |
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