Acrylamide → Acrylamide

HRID 1105495

反応式

HRID 1105495 の反応式
[C:1]([OH:5])(=[O:4])[CH:2]=[CH2:3].[C:6]([NH2:10])(=[O:9])[CH:7]=[CH2:8].[C:11]([O:15][CH2:16][CH:17]([OH:19])[CH3:18])(=[O:14])[CH:12]=[CH2:13].S(OOS([O-])(=O)=O)([O-])(=O)=O.[NH4+].[NH4+].S([O-])(OCCCCCCCCCCCC)(=O)=O.[Na+:49].[OH-].[Na+]>CO.CC(C)=O>[C:1]([O-:5])(=[O:4])[CH:2]=[CH2:3].[Na+:49].[C:11]([O:15][CH2:16][CH:17]([OH:19])[CH3:18])(=[O:14])[CH:12]=[CH2:13].[C:6]([NH2:10])(=[O:9])[CH:7]=[CH2:8]

参加物

10

反応物 6

HCID 6579AcrylamideHCID 6581Acrylic AcidHCID 14798Sodium HydroxideHCID 612492-Hydroxypropyl acrylateHCID 62648Ammonium PersulfateHCID 3423265Sodium Lauryl Sulfate

生成物 2

HCID 6579AcrylamideHCID 86737734Sodium acrylate 2-hydroxypropyl acrylate

試薬・触媒・溶媒 2

HCID 180Acetone溶媒HCID 887Methanol溶媒

実験手順

A terpolymer of sodium acrylate-2-hydroxypropyl acrylate and acrylamide was prepared utilizing an emulsion polymerization process. The mole ratios of acrylic acid to acrylamide, mole percent of 2-hydroxypropyl acrylate and molecular size were varied by controlling the reaction parameters. Six representative samples of the terpolymer were prepared with the compositions of the various terpolymers being estimated based upon their total nitrogen content. In the reaction, ammonium persulfate was utilized as the polymerization initiator or catalyst. Reagent grade acetone and reagent grade anhydrous methanol were utilized to form the solvent. The emulsifier was sodium lauryl sulfate, and 2 N aqueous sodium hydroxide was utilized to neutralize the reactants. The dried products were thereafter milled and passed through a number 30 mesh screen. The reaction was conducted over a period of three hours at a reaction temperature of about 60° C.

後処理

  1. customan emulsion polymerization process
  2. customthe reaction parameters
  3. customSix representative samples of the terpolymer were prepared with the compositions of the various terpolymers
  4. customto form the solvent
  5. customThe dried products were thereafter milled

出典と根拠

ORDレコード
ord-bba8ba5f4c674effba9024936ea21e88
出典データセット
uspto-grants-1982_01
特許番号
US04309329

関連ノート

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