Homopolymer nanoparticles by self-emulsion polymerization reaction and preparation method thereof
US-10093752-B2 · Oct 9, 2018 · US
US11919978B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11919978-B2 |
| Application number | US-201817257318-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 27, 2018 |
| Priority date | Dec 14, 2018 |
| Publication date | Mar 5, 2024 |
| Grant date | Mar 5, 2024 |
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A hydrate kinetic inhibitor, which is prepared by a polymerization of mercaptoethanol and N-vinylcaprolactam, is hydroxyl terminated poly(N-vinylcaprolactam) having a structure of formula (I) below, wherein n=10 to 1000. The inhibitor is a novel hydrate kinetic inhibitor, which has low effective concentration and high cloud point, and is effective when the degree of supercooling is relatively high.
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We claim: 1. A method for producing a hydrate kinetic inhibitor, wherein the hydrate kinetic inhibitor is hydroxyl terminated poly(N-vinylcaprolactam) having a structure of formula (I), and n=10 to 1000, the method comprising: sequentially adding a chain initiator, a N-vinylcaprolactam, a mercaptoethanol, and a isopropanol into the reactor, wherein the molar ratio of the mercaptoethanol to the N-vinylcaprolactam is 1:20, the chain initiator is azobisisobutyronitrile, a molar ratio of the azobisisobutyronitrile to the N-vinylcaprolactam is 0.01:1, and a solid-to-liquid ratio of the N-vinylcaprolactam to the isopropanol is 1:15 g/mL, and stirring until dissolved; sealing the reactor using a rubber plug, and performing three cycles of vacuumizing and introducing nitrogen; reacting under the nitrogen atmosphere at 85° C. for 24 hours to obtain the reaction solution; drying the reaction solution by the rotary evaporation at 50° C., and cooling to the room temperature to obtain the crude product; dissolving the crude product in tetrahydrofuran and precipitating using n-hexane to obtain a precipitate; washing the precipitate with anhydrous ether, and sieving and drying to obtain the hydrate kinetic inhibitor.
by a heterocyclic ring containing nitrogen · CPC title
Introducing sulfur atoms or sulfur-containing groups · CPC title
Compounds containing carbon-to-nitrogen triple bonds · CPC title
organic depositions, e.g. paraffins or asphaltenes · CPC title
taking place solely at one end or both ends of the polymer backbone, i.e. not in the side or lateral chains · CPC title
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