Ethylene → HCID 86739097, compound

HRID 648362Notes

Reaction equation

HRID 648362 reaction equation
C=C.[C:3](OC)(=O)[CH:4]=C.[C:9]1(=[O:15])[O:14][C:12](=[O:13])[CH:11]=[CH:10]1.C(OC(OOC(OC(CC)C)=O)=O)(CC)C>CO>[CH2:3]=[CH2:4].[C:12]([O:14][CH3:9])(=[O:13])[CH:11]=[CH2:10].[C:12]1(=[O:13])[O:14][C:9](=[O:15])[CH:10]=[CH:11]1

Participants

6

Procedure

6.34 kg/h of ethylene plus 1.06 kg/h of liquid monomers containing by weight 97.2% methyl acrylate (MA), 2.7% maleic anhydride and 0.1% butylated hydroxy toluene (BHT) as well as 0.2-0.3 kg/h of methanol as telogen were fed continuously to a 720 ml adiabatic continuous stirred tank reactor. Reaction was initiated and maintained by the addition of di(sec-butyl)peroxydicarbonate (20% PDC/80% t-butylbenzene). Reaction conditions: Reactor temperature=160° C., Feed temp.=25° C. Pressure=186 MPa, Total monomer conversion=15±1%. Comonomers were introduced into the hot reactor at appropriate reactor pressures to avoid phase separation. Approximately 6.5 kg of E/MA/maleic anhydride polymer was made with a measured composition of 46.5/51/2.5 wt % and a melt flow rate (2160 grams weight, 190° C.) of 7-9.

Workup

  1. customwere fed continuously to a 720 ml adiabatic continuous stirred tank reactor
  2. customReaction
  3. customReaction conditions
  4. customtemperature=160° C., Feed temp
  5. custom=25° C
  6. additionComonomers were introduced into the hot reactor at appropriate reactor pressures
  7. customphase separation
  8. customa melt flow rate (2160 grams weight, 190° C.) of 7-9

Sources & evidence

ORD record
ord-c155198ea0c24eafbff1fd330cfb4316
Source dataset
uspto-grants-1983_10
Patent number
US04412043

Reaction notes

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