Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2418960Generated: November 2, 2026

Azobisisobutyronitrile → Sodium acrylate

https://huagongshe.com/reaction/2418960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantAcrylamideHCID 6579—
ReactantAcrylic AcidHCID 6581—
ReactantSodium HydroxideHCID 14798—
ReactantSpan #80 (Sorbitan monooleate)HCID 70693544—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductAcrylamideHCID 657935%
ProductSodium acrylateHCID 406853365%

Reaction Conditions

Temperature60 °C

Reaction Steps

In the manner described for the preparation of dispersion A, 20 parts of ethoxylated nonylphenol (degree of ethoxylation 8 to 12) and 53.3 parts of sorbitan monooleate are dissolved in 347 parts of a mixture of 84% of saturated aliphatic hydrocarbons and 16% of naphthenic hydrocarbons (boiling range of the mixture 192° to 254° C). There is then added a solution of 133.6 parts of acrylamide and 59 parts of acrylic acid in 389.4 parts of water, the pH of which has been adjusted to 8.0 with 18 parts of sodium hydroxide, and the aqueous solution is emulsified in the hydrocarbon oil. Nitrogen is passed over the mixture for 30 minutes and the mixture is then heated to a temperature of 60° C over 15 minutes. At this temperature, a solution of 0.212 part of 2,2'-azo-bis-isobutyronitrile in a little acetone is added. Polymerization is complete after heating the mixture for 3 hours at 60° C. There is obtained a coagulate-free sedimentation-stable dispersion of a copolymer of 35% of acrylamide and 65% of sodium acrylate. The K value of the polymer is 247.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04104226
Source datasetuspto-grants-1978_08
ORD IDord-e17cb38b67854720974b2cdc9ee9e89e
Source noteuspto-grants-1978_08