Vinyl Chloride → Vinyl chloride-vinyl acetate

HRID 876099

Reaction equation

HRID 876099 reaction equation
[CH:1]([Cl:3])=[CH2:2].[C:4]([O:7][CH:8]=[CH2:9])(=[O:6])[CH3:5].S(OOS([O-])(=O)=O)([O-])(=O)=O.[K+].[K+].C(OS(C1C=CC=CC=1)(=O)=O)CCCCCCCCCCC.[Na]>O>[C:4]([O:7][CH:8]=[CH2:9])(=[O:6])[CH3:5].[CH:1]([Cl:3])=[CH2:2]

Participants

6

Conditions

Temperature
60 °C

Procedure

Deionized water (600 g), a monomer mixture composed of 438.8 g of a vinyl chloride monomer (97.5% by weight based on total charge monomer amount), 11.2 g of vinyl acetate (2.5% by weight based on total monomer charge amount), and 2.25 g of potassium persulfate were charged into a 2.5-L autoclave. The reaction mixture was stirred with a stirring blade while maintaining the rotation speed at 120 rpm, and the temperature of the reaction mixture was raised to 60° C. to start a polymerization. A 5% (by weight) aqueous solution of sodium dodecylbenzenesulfonate (180 g, 2% by weight based on total monomer charge amount) was continuously added from the start of the polymerization to 4 hr after the start of the polymerization, and the polymerization was stopped when the polymerization pressure was dropped by 0.6 MPa from a saturated vapor pressure of the vinyl chloride monomer at 60° C. Thereafter, the residual monomer was recovered to obtain a vinyl chloride-vinyl acetate emulsion.

Workup

  1. additionwere charged into a 2.5-L autoclave
  2. temperaturewhile maintaining the rotation speed at 120 rpm
  3. customa polymerization
  4. customafter the start of the polymerization
  5. customthe polymerization pressure
  6. customThereafter, the residual monomer was recovered

Sources & evidence

ORD record
ord-4226907c530e4fd9940da8fa32d68df8
Source dataset
uspto-grants-2015_03
Patent number
US08986796B2

Linked notes

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