반응 #446966

ord-2ae7de8432c643b5b4fd18835008ff73

반응 방정식

C=CC(=O)NC(C(C)C)S(=O)(=O)[O-].[Na+]
sodium acrylamido-2-methylpropane sulfonate
C=CC(N)=O
acrylamide
C=CN1CCCC1=O
N-vinylpyrrolidinone
C=CC(=O)NCCCCCCCCCCCCCCCC
N-Hexadecylacrylamide
CCCCCCCCCCCCOS(=O)(=O)[O-].[Na+]
sodium dodecylsulfate
C=CC(=O)NC(C(C)C)S(=O)(=O)[O-].C=CC(=O)NCCCCCCCCCCCCCCCC.C=CC(N)=O.C=CN1CCCC1=O.CC(=O)N(C)C.[Na+]
N-Hexadecylacrylamide Acrylamide DMA N-Vinylpyrrolidinone Sodium Acrylamido-2-methylpropane sulfonate

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타fitted with a chilled water condenser
  2. 2
    기타and polymerization
  3. 3
    여과filtered
  4. 4
    기타dried under vacuum at 30 C

실험 절차

A solution was prepared of 6.0 g of sodium dodecylsulfate in 300 mL of deoxygenated water. N-Hexadecylacrylamide, 0.666 g, was dissolved in this solution followed by 9.44 g of acrylamide, 8.92 g of DMA, 10.00 g of N-vinylpyrrolidinone (NVP) and 27.99 g of sodium acrylamido-2-methylpropane sulfonate. The resulting solution was carefully transferred to a 1 L Morton style resin kettle fitted with a chilled water condenser, thermometer, inert gas sparger and mechanical stirrer. The temperature was adjusted to 25 C. and polymerization was initiated by the addition of 0.0518 g of 2,2'-azobis(N,N'-dimethylene-isobutyramidine) dihydrochloride. After stirring for 16 hr at 25 ±0.2 C., a 250 mL portion of the viscous solution was added to 3 L of acetone. The precipitated polymer was then masticated in a Waring blendor with methanol/acetone, filtered and dried under vacuum at 30 C. The yield of polymer was 42.21 g.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05003000uspto-grants-1991_03