Alpha-Methylstyrene → alpha-Methyl styrene-acrylonitrile

HRID 2109318

Reaktionsgleichung

Reaktionsgleichung von HRID 2109318
C[C:2]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)=[CH2:3].[C:10](#[N:13])[CH:11]=[CH2:12].[C:14](OOC1(OOC(C)(C)C)CC(C)CC(C)(C)C1)(C)(C)C.C(OOC(C)(C)C)(C)(C)C>C1(C)C=CC=CC=1>[CH3:12][C:11](=[CH:14][CH:3]=[CH:2][C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1)[C:10]#[N:13]

Komponenten

6

Versuchsvorschrift

70 parts by weight of alpha-methylstyrene, 30 parts by weight of acrylonitrile, 5 parts by weight of toluene, 0.135 parts by weight of 1,1-bis (tert-butylperoxi)-3,3,5 trimethylcyclohexane and 0.015 parts by weight of di-tert-butyl peroxide were homogenously mixed and continuously introduced to the reactor. The polymerization was carried out as the reaction temperature was kept at 110° C. After completion of the polymerization, the resulting polymer was supplied to a vaporizer equipped with a heat exchanger, kept at a temperature of 250° C. and a pressure of 20 Torr, in which non-reacted monomers and solvents were removed. Then, the polymer was palletized through an extruder equipped with a discharge pump. The alpha-methylstyrene-acrylonitrile copolymer prepared by the above method had an average molecular weight of 9.5×104 and a glass transition temperature (Tg) of 125° C.

Aufarbeitung

  1. additioncontinuously introduced to the reactor
  2. customwas kept at 110° C
  3. customAfter completion of the polymerization
  4. customequipped with a heat exchanger
  5. customkept at a temperature of 250° C.
  6. customa pressure of 20 Torr, in which non-reacted monomers and solvents were removed
  7. customequipped with a discharge pump
  8. customThe alpha-methylstyrene-acrylonitrile copolymer prepared by the above method
  9. customa glass transition temperature (Tg) of 125° C.

Quellen und Nachweise

ORD-Eintrag
ord-447b08bba624437ba3ad8faa32450b12
Quelldatensatz
uspto-grants-2009_04
Patentnummer
US07514502B2

Verknüpfte Notizen

Wird geladen…